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Introduction

On starting to pave the road for our diagnostic kit we needed to envision and design a complete roadmap guided by:-

●                   Extensive Analysis To The Market We are entering

●                   The Current State Of Our Nation

●                   Defining and Refining our customer segment,their market share,expected growth

●                   Understanding Our Competition

●                   Gaining more information from the people regarding the current situation

●                   Searching for the Stakeholders & Those who could contribute to our project

●                   Designing a Business Model Canvas & Sustainability

●                   Preparing a Market Plan for our diagnostic kit and platform.

 

Problem  Definition

Inborn errors of metabolism (IEM) are one of the biggest problems that face newborns & children especially if the child is not detected to have one of them.

 

Phenylketonuria is an autosomal recessive (AR) disease that causes a decrease in the metabolism of Phenylalanine(Phe). And if Phe accumulates undetectably a child can have dramatically negative sequelae that could end in very harmful complications such as mental retardation and neurological problems.


Unfortunately the current screening of phenylketonuria to newborns got a lot of drawbacks, One of the biggest is its high cost which isn’t affordable by a lot of people especially in developing countries, however, if phenylketonuria is detected early the patient could survive by sticking to a very strict diet which tremendously affects his  quality of life in a negative way. So we had to do something  to help them.

Product Overview

P-Kit: Point Of Care Home Screening Test Kit

In designing our kit we are working on, turning our screening tool into a home based tool that can be used by any person. We knew that our ultimate goal would be for our screening kit to reach every house and family here in the county so the kit needs to be available to be used at any time ,and making it as simple to use as possible is a top priority, that's why we went through making the kit be designed as a lateral flow assay, with the inclusion of a clear manual to help the user get proper and accurate results.

P-Pill: A Next Step Therapeutic Treatment for PKU Patients

As we come to acknowledge that diagnosed PKU patients have to stick to very strict diets for the sake of their survival making them deprived from many types of food as well as being forbidden from many drugs that contain phenylalanine and therefore have a generally lower quality of life so we needed to think and devise a solution for them.


Therefore In the future we envision that our therapeutic approach will be in the form of an enteric coated pill and this pill would need to be used life-long as the patient would be taking this pill every specified duration of time and this pill would help his body to provide the missing enzyme in his body therefore making him able to live a normal life and be able to enjoy their life normally .

SWOT analysis

 

Rest ASSURED: How we were inspired by WHO STD Diagnostics initiative (SDI)

 

Earlier on we knew that the WHO have developed and created a criteria for future diagnostics made in the field of Sexually Transmitted Diseases (STDs) and as they made these criteria specifically for people and countries with limited resources, Designing ASSURED:  affordability, sensitivity, specificity, user-friendly, rapid and robust, equipment-free and deliverable.


And we were inspired by them as we consider this to be a future benchmark and guideline for all point of care diagnostics and especially ours to help us in the creation more of a quality tested product and sustainable program for the prevention of further misdiagnosis of inborn errors of metabolism in general and more specifically phenylketonuria.

 

●    Affordability:

First point we have regarded in designing our product was to make our product as affordable as possible and to achieve that endeavor we have worked on always researching lesser value material without compromising the accuracy of our kit which was done by replacing the use of microfluidics with lateral flow assays and the replacement of the use of antibodies with aptamers.

●    Sensitivity & Specificity:

In all our work Accuracy was one of the essential pillars that we couldn’t compromise that’s why we have included the use of aptamers as they are generally more stable than antibodies can act like monoclonal antibodies and can even detect non-immunogenic substances in addition to the use of logic gates within the circuit that ensure specific binding to the target molecule and higher sensitivity.

●    User-Friendly:

Our kit was designed on the basis of being an easy to use device ,and in order to do that we picked a simple method for the patient to be able to self test himself/herself accompanied by a clear guide for the customer to easily understand the test result.

●    Rapid & Robust:

Our use of lateral flow assay accompanied by our robust design and usage of multiple controls and presence of a valid detection system ensures both rapid & accurate results.

●    Equipment-Free:

Our Device is labeled equipment-free needing nothing more than the actual kit and a drop of blood to get the results you need ensuring ease of use and avoiding complexity.

●    Deliverable:

Our plan is to provide our kit as a home device that would be easily present through either direct online ordering from our website or by mass distribution to pharmacies all across the country. We plan for this to begin by contacting owners and negotiating a long-term plan for the kit to be presented and featured at their places.

 

 

Market Analysis

 

Current National situation

To analyze our market properly we needed to understand the current situation here in our country first, so we tried to find out how much were our people interested about the topic of phenylketonuria & Screening tests ,and after thorough analysis of the results it became clear that there were a fundamental problem as the interest level about the topic have been decreasing through the years, as we have witnessed the levels of interest and searches having a share of 1.0k of the volume of searches out of 89.3K searches about the disease. All of which might indicate lack of knowledge about the disease.

Figure (1). Generated Data Using Google Trends tool regarding search interest about phenylketonuria keyword between 2004-present in Egypt.

Figure (2). Data Generated Using SemRush tool regarding search volumes worldwide of phenylketonuria keyword

 

Further search and analysis also demonstrated that Egypt’s interest compared to other countries worldwide was disappointing being in the 26th Position ,and with the knowledge that Egypt is one of the highest countries with Inborn errors of metabolism & Phenylketonuria as according to data & research 1 out of every 5000 live births here turns out to be affected with phenylketonuria and even this data might be presenting an underestimation of the data.

 

We can combine the meaning of all that we now know to conclude that our people need much more information about the topic than they already know ,and that the current awareness regarding the situation is low, also we can conclude that our screening kit for diseases such as phenylketonuria will have a large section of users that will need both information and the facilities to access Medical care that they didn’t know they need.

Figure (3). Data showing worldwide search interest about phenylketonuria keyword categorized by region between 2004-present

 

In addition, our country’s current policies endorsed by the president now goes in line with working on finding a solution for inborn errors of metabolism as the government is trying to find new initiatives to help with the current problem. Therfore we expect a substantial rise of the public’s interest in the topic which would increase the market’s size and change their buying habits.

 

Pharmaceuticals Market analysis: A Broad View of the Market

 

Figure (4). Market overview for pharmaceuticals industry using Open Trends tool

 

After Further analysis of our market we found that it's a relatively easy market to compete in here in Egypt as it had an estimated difficulty of competition of 5%. On the other hand We have found out that although the market have an average high traffic of 8.2 million with peaks in the market that reached up to 50 million, that growth has dramatically decreased from the previous year with a negative Year-over-year (YOY) growth of - 143.07%, However we believe the lack of competition and market traffic would compensate for the decline in yearly growth.

Figure (5). Market overview for pharmaceuticals industry using SEMRush tool

 

Furthermore  we have found that the pharmaceuticals market had such a large market size here in egypt with a substantial 199.3M of Revenue as a total addressable market however only 14.3M was the serviceable available market. This indicates that the market has a great potential for expansion allowing new competitors the chance to gain much more revenue.

 

 

Competitor & Niche Market Analysis

Revealing a gap in the market

In Egypt, We have one of the highest prevalences of phenylketonuria in the whole world which was measured to be around 1 for every 5000 child. And it would be expected for our country to have a greater number of facilities and tests for these children and their screening to prevent a little child from getting long-term brain damage.


However the actual situation is remarkably different from what is expected as here in the country there are only very few providers of screening services and diagnostics, until very recently with the government's initiative to counter Inborn errors of metabolism, and
practically, there is complete absence of any point of care diagnostic in the market for any inborn error of metabolism.

We designed the heat map below to demonstrate the prevalence of PKU Worldwide according to literature, and as it can be seen Egypt is one of the few countries in the map to have the darkest color concentration, all of which indicates a huge gap between what is happening and what needs to be done.

Competitors in the current scene:

Diagnostic Approach Competitor Analysis

After thorough investigation of the market and the demand we have found out that in the country there is only two tests available that can diagnose the disease which are:

●       National Gene sequencing: in which they analyze the DNA sequence for patients in order to find out the presence of changes in areas of the genome that would represent the person acquiring the disease.

●       Tandem mass spectrometry


However we’ve found out that our competitors lack many things:

●       First of all, our competitor tests in the country are very costly as a single test for phenylketonuria done through the national gene sequencing program is estimated to cost around 150$ and the tandem mass spectrometry would cost around 25$ knowing that here in Egypt we have an average salary of 500$ per month. So these tests would be very expensive for the average user especially knowing that we are targeting more of the lower income parts of the society as they are more likely to be unaware of that illness and have much higher rates of home deliveries for children.

●       The Second issue regarding these method is their extensive need for human resources and computing which is required to interpret and analyze the data with the current workflow

●       The Third issue regarding a method such as the gene sequencing is the need for a very large disk and computer storage space with it being a hurdle to both long-term data presence and the use of very high disk space.

●       The Final issue would be the time factor as these tests take a long time

 

 

Figure(7). Showing a double axis competitor analysis showing likely testing competitors categorized according to perceived quality & Price

 

 

 

Therapeutic Approach Competitor Analysis

 

After thorough investigation of the market and the demand we have found out that there is two general management and treatment modalities  available that can help treat the disease which are:

 

●Dietary Restriction: By Generally eliminating and forbidding foods and drugs that contain phenylalanine

 

● Sapropterin (Kuvan) : Which is a drug that can activate residual PAH enzyme to improve metabolism of phenylalanine


But on the other hand we’ve found out that other modalities have major drawbacks such as :-

 

● Sapropterin (Kuvan) isn’t effective in all patients with pku and have varying effects in these patients according to the amount of residual PAH enzyme in the patients

 

●Sapropterin (Kuvan) drug have various side effects such as esophagitis, gastritis, headache, vomiting, runny nose and nasal congestion, sore throat, diarrhea, and cough

 

●       It’s easy to recognize how much severe dietary restrictions would affect a child or a later on adult with PKU and the drawbacks of the restriction of so many types of food and drugs and how it would affect his quality of life

 

StakeHolder analysis : Identify, Prioritize & Understand

Identify

The first thing that we need to do when conducting a stakeholder analysis is the identification of all those that currently & could possibly in the future influence your project so as to achieve that endeavor.

-        World Health Organization (WHO)

-        National PKU Alliance

-        Egyptian Health Ministry & Government Officials

-        Egyptian PKU Association

-        Public & Private Hospitals

-        UK’s National Society For PKU Charity

-        Private Clinics & Doctors

Prioritize

Next on we needed to Prioritize our stakeholders and their rules and prepare proper management for each stakeholder either on an individual or organizational level and in order to do that we designed a Power/Interest grid to establish each role and prepare a project management plan in advance.



 

 

Understand

And In order to do this we needed to answer 3 questions:-

 

What motivates our stakeholders?

Our stakeholders are motivated primarily by the very fact that by helping our project and our cause they are acting out and being proactive towards a societal and a devastating national problem that have been lurking around for so long. Our stakeholders see the potential of such a project and its long term impact both locally and internationally.They are motivated because they can help in the formulation of a solution to help ease the suffering of others and hopefully to one day prevent any future pain of a misdiagnosed child.

How does our project align with their priorities?

Those who already influence our project or could potentially support our cause & product are those that have their main priorities set as being:-

●       Achieving Universal & National Health Coverage

●       Promoting Health & Well being of humans

●       Working Towards solving the problem of IEMs & PKU

And Our Projects main goals align with their same priorities as we aim towards providing a national and maybe an international solution for an unsolved and ongoing problem and possibly provide them with a long term

How can we change any negative views about our project?

When we are approached by negative view we need to:

●       Meet them one on one and establish early contact and try to explain misunderstood points

●       Listen to what they say non judgmentally and try to seek information and opinions from them so we can further enhance our project

●       Learn from what they think and see a middle solution that would work to solve both their problem and ours.

 

Investments in PKU & Probable Sources of Funding

We found after search that there have been minimal investments in the field of finding a treatment for PKU, However we found out that the main two investments in the field was done by:-

 

-        Pfizer pharmaceutical company which invested 60 million $ in supporting gene therapies for PKU, More specifically for a company called Homology Medicines which work on genetic medicines

-        The National PKU alliance has also, according to their page, worked on investing in targeted research in PKU.

 

So we have tried to learn from them and as we see we can think that Pfizer company & National PKU alliance could be potential sources for funding but on the other hand other key players that was identified in the stakeholder analysis could also be suggested as potential sources of funding for our project such as the Egyptian PKU alliance & The health ministry.

 

Long Term Plan: Business Model Canvas, Cost analysis, Marketing plan & Timeline

 

 

Our Business Model Canvas

Diagnostic Kit Business Model Canvas

 

 

Therapeutic approach Business Model Canvas

 

 

 

 

Cost analysis

To try and make an estimate of what the cost of our product and one test would be we went on to estimate the expected product using literature, similarly made products, and lateral flow assays as well as the prices which we paid for our lab work, and to make estimates of how much each of them would be needed to hypothetically manufacture one piece of our product

 

Figure(8). This figure illustrates the cost share of each of our lateral flow assay diagnostic

 

 

 

 

Needed Components

Estimated cost by EGP for what is needed to make one test

Vivid Plasma Separation Model

16 EGP per test

Aptamers & E-coli DH5α

15 EGP per test

Desicant

5 EGP per test

Membrane backing

4.5 EGP per test

Plastic Housing

2.5 EGP per test

Foil-lined Pouch

5 EGP per test

Adhesive

0.5 EGP per test

Laminate Sheets

0.5 EGP per test

Whatman Chromatography paper

1 EGP per test

Manufacturing & Manpower

4 EGP per test

Total cost per test

49 EGP per test

 

So after investigation it is estimated that the total cost of our product would be around 49 EGP per test which is the equivalent of 2.5$.

This indicates that our product would be much cheaper than its competitors with the tandem mass spectrometry being priced at 25$ and the national gene sequencing program which is priced at 150$.

Marketing plan

 

In the making of our bioentrepreneurship we know that it was essential to design a comprehensive marketing plan for it since we knew that few biotechnology companies fail to recognize the importance of proper marketing of their products to achieve both short and long term success.

Who are we going to target?

Our Ideal Target Persona

In the path to market our product we first off need to recognize what are our Ideal customer or target persona so we designed a complete profile of who our targeted clients might be.

 

How are we going to Market Our Product ?

Our Marketing Channels

In deciding our marketing channels we looked into our people, our thoughts of our target persona & common channels that people use and we diversified our target channels into three main types:
          - Digital Channels

          - Traditional Marketing

          - Product awareness outreach Campaigns

Digital Channels

In designing our digital marketing framework we plan to work on 3 main outlets which are:

 

Social Media Channels

First off we are going to start by making a Content plan for Famous social media channels such as Facebook, Instagram & Twitter followed by using both earned and paid advertisement to drive product awareness about our product.

Website, SEO & SEM

We are planning to launch a website for both our Diagnostic & Therapeutic approach once they pass the stages of clinical trials and get certified and we would be working on both On-site & Off-Site Search engine Optimization(SEO) to drive the highest possible organic traffic to the website combined with keyword planning and working on link building campaigns and addition of backlinks and removing faulty ones to increase our page search engine ranking. Also we are planning to start using search engine advertising using google ads.

 

Traditional Marketing

We would mainly rely on traditional marketing on two types of advertising which would be print advertising such as that done in magazines and newspapers as we know that a large proportion of our customers would be people who rarely use their phones and are generally lower in socioeconomic status

Also we intend to work on Television and radio advertising as we are aware that a sizeable proportion of people in our country are illiterate as well as those with either visual or auditory defects therefore we need both spoken and visual advertising to reach all the people in our society and work generally on brand awareness & interest.

 

Product awareness outreach campaigns & Charity

To reach the final proportion of our target groups we intend to launch outreach campaigns to people that either have in accessibility to normal methods of contact as well provide them with either discounted or completely free products as well as provide education to those unaware of the current situation.

 

 

 

 

Timeline

 

In order to be able to envision our future we conducted a timeline for the next 10 years with the main steps that we would need to do in order for our therapeutic and diagnostic approaches to reach the market.


 

 

 

 

 

 

 

National Regulations, Intellectual Property & Obtaining a patent

 

Introduction


Maybe we are not men of the law however as we know the importance of knowing the legislations and national regulations we worked hard to understand the full path we are going to need to walk through to accomplish our target of turning our Therapeutic & Diagnostic platform into real life we conducted extensive research on all the laws and regulations that would be on our way to be able to protect our work and try to ensure its future success in addition to preparing a plan on how we could possibly get the required certificates & documentation as well as acquire patency of our platforms.



Commonly used abbreviations:

Egyptian Drug Authority = EDA

Institutional review board = IRB

Investigator’s Brochure = IB

good manufacturing practice = GMP
Good Lab Practice = GLP

Good Clinical Practice = GCP

Contract Research Organization =CRO

Curriculum vitae = CV

In Vitro Diagnostic = IVD

In Vitro Diagnostic Regulations = IVDR

Post-Market Surveillance = PMS

 

 

 

Intellectual Property & Obtaining a patent

 

In order to turn our project into reality we needed to work on how to obtain a patent for our work to protect our intellectual property so our research began and we worked on acquiring the knowledge how to do so.

 

First of we started by finding whether our desired kit an pill would be patentable or not and we found out that Although methods of diagnosis and treatment of humans can’t be patented, Genetically engineered microorganisms and processes by which a biological material is produced and pharmaceuticals ( of which our therapeutic approach fall under ) are patentable as well as part of our diagnostic kit which is the engineered circuit able to detect Phenylalanine with specificity and sensitivity.

 

 

Then we went through the process of finding out what we would need to do and pay in order to be able to acquire patency and we found out that we need to fill in a form as presented in the figure below.

Figure(8). The Egyptian Patent office, Patent request application & Temporary protection

 

And After More Search we have found out that patents last for 20 years with yearly increasing fees starting from 20 EGP annually and reaching 1000 EGP starting from the 17th year as well as extra fees for filing the application ,expert reviews & etc.

 

 

Essential Documents & Preparations Required for Accreditation from EDA

 

In Pre-clinical Trials

1.       A cover letter directed to the administration of clinical trials signed & dated clarifying :

●        Applicant request, Product information (PI))

●        Table of all submitted documents.

●        Aim of submission, proposed human use, dosage, strength, and route of administration with an overview of the nonclinical testing strategy.

2.       Official delegation letter: stamped, signed and dated from sponsor to the representative person who will submit the documents and deal with Bio Inn-EDA.

3.      institutional review board (IRB) Approval.

4.      Investigator’s Brochure(IB)

5.      Signed agreement/ contract between involved parties

6.     Signed declarations by Investigators.

7.      CV & relevant documents evidencing qualifications of the investigator

8.     Investigational medicinal product dossier.

9.     Certificate(s) of analysis of the investigational product

10.  The quality and safety of preclinical preparations should follow the strict control of the manufacturing process following the principles of GMP

11.    Name of the laboratory, address, and telephone number with a list of all tests conducted in each laboratory.

12.   Evidence of accreditation and documented evidence of GLP compliance of the designated laboratories to be used for the assay of preclinical samples.

13.  Complete detailed preclinical studies reports for the investigational medicinal product are required to be submitted:

●        Good Laboratory Practice (GLP) compliance of the studies

●        Specification of the test material.

●        Reports on studies: Pharmacology, Pharmacokinetics & Toxicology

14.   Full, legible copies of the key, peer-reviewed published articles supporting the application.

15.   The Preclinical data submission as one hard copy and one soft copy

16.  Fees proof of payment: Fees are 15,000 LE.

 

In Clinical Trials

After Filling of “Applicant request to the Egyptian Drug Authority For Clinical Trial Authorization on a medicinal product for Human use"” multiple documents would be needed in our country to start clinical trials such as:-

-        Ethical committee approval and for us to get this approval we would need to supply them with our protocol version & amendments if present

-        Investigator’s Brochure, Which is a combination of clinical & non clinical data on the product investigated in the clinical trial and contains info to provide easier understanding of the rational & key features about the protocol of the clinical trial & safety measures taken
-A signed and Detailed Document prepared under and according to ICH Guideline for Good Clinical Practice(GCP)

-        Information Provided to Trial Subjects including an:-
⚫ An informed consent form with translations in both arabic and english
⚫
Any Other Written Information
⚫ Advertisement for subject recruitment: To document that recruitment measures where appropriate

-        Insurance statement that any trial-related injury will be compensated

-        Signed agreement contract between:-
Institution & Sponsor
Institution & Contract Research Organization (CRO)
CRO & Sponsor

-        Dated & Documented Favorable Opinion of Ethics Committee of national registered IRB

-        Documents showing evidence of qualifications of whom investigator tasks are delegated

-        Valid GMP Certificate for both the investigational product and placebo if used

-        And Finally Proof of payment of 50,000 EGP in protocol submission and 30,000 EGP in case of Amendment submission

As well as other requirements regarding certification,Other regulatory processes,etc.

-       

Getting GMP Compliance Accreditation

 

As we knew that any one who manufactures medicine that is intended for the EU market, must comply with GMP. we started to understand and get information regarding it as GMP ensure the quality and the safety of the medications, dietary supplements, certain best practices in the manufacturing, packaging, and labeling of pharmaceuticals and covers all aspects of the production process and must be followed to take GMP certificate & accreditation

.

We intend to get GMP Accredited by following basic recruitment for EU-GMP to meet a high level of compliance through self-evaluations of standard operating procedures, comprehensive facility inspections, or audits, as well as GMP-related documentation.

 

Basic GMP recruitment:

1.       Product quality review should be applied in fixed time frames; these time frames can be adjusted based upon manufacturing and campaign duration with adequate justification.

2.      In order to avoid the routine use of metal detectors, the company must demonstrate that it has identified and managed the risks.

3.     Risk-based prevention of cross-contamination in production.

4.      An audit conducted by the manufacturing-authorization holder itself should be integral to the manufacturer's quality-assurance system.

5.      More than one batch number appears on the packaging of medicinal products.

6.     The supply chain for each active substance must be established back to the manufacture of the active substance starting materials.

7.      For patching the product we should follow the Quality Risk Management (QRM) criteria:

●        length of time the equipment has been in use

●        Phamatolucical form of the drug product that cannot be homogenized (tablet, capsules, etc)

●        the expiry date of the drug products

●        ongoing stability study design and results

●        reference samples plan for each batch

●        criticality of the drug product and the risk of shortage that may arise from any quality issue

●        prior approval of the MAH

8.     Medicinal products that are relabelled or repacked with the purpose of parallel trade should be in compliance with any specific national legislation or guidance in relation to the batch number(s) that are to be present on the parallel distributed traded packs.

 

Finally to get GMP certification all this process should be inspected by a supervisory authority or EEA competent authority if the first one wasn’t able to be inspected for any reason upon our request.

 

And as we aspire that in the future our diagnostic kit would be completely manufactured locally here in egypt we needed to understand the regulatory system in here and to know the steps of:

In Vitro Diagnostics registration in EDA

 

In locally manufactured products

First we needed to provide EDA with some general documents regarding our diagnostic such as:-

 

●        Receipt of payment for services

●      An official application from us stamped & signed by our future company

●  Document representing formal pledging to abide by safety mechanisms

●     Commercial register & Tax Card

 

Then we need to provide them with some technical details for documentation regarding:-

-    Device description:  Such as Name of the device, Brand name,Intended use,Risk classification according to European regulations & finally Description of the principle of the assay and methodology used. - Description of individual components included in the IVD.

-  Device history: If it had history of production in the market or any other countries. And summary of any adverse effects, recalls & corrective/preventive actions

-    Risk analysis and control summary.

-    Design and / or manufacturing information.

-     Clinical evidence report & Summary (If IVDR applied).

-     Performance evaluation: Such as Diagnostic Sensitivity & Specificity done in phases of clinical & preclinical trials

-   Product Validation and Verification: which is represented by Analytical Sensitivity & Specificity, Measurement of the range of the assay,Verification & Validation of instrumentation & Accuracy (Represented by Reproducibility & Repeatability)

-    Labeling: Inner & Outer Labels, Instructions for use & any advertising material

-         Manufacturing process and control.

-         In-process inspection and testing.

-         Finished product assembly and testing reports.

-         Product release process and statement of compliance.

-         Manufacturer testing reports

-         Commitment to follow up with medical device PMS.

References

  1. Matar, Amal, and Henry J. Silverman. "Ethical Analysis of Egypt's Law Regulating Clinical Research." Journal of Empirical Research on Human Research Ethics (2022): 15562646221096188.


  2. How to bring a medical device to market in Europe - Leon Research: Cro - clinical trials Spain, Italy and Portugal (2022) Leon Research | CRO - Clinical Trials Spain, Italy and Portugal. Available at: https://leonresearch.com/medical-devices-europe-mdr-2017-745/


  3. Reliance procedures during Registration of Biological products at EDA (2022) central Administration For of biological products & clinical trials, Available at:https://www.edaegypt.gov.eg/media/lrqnmu0v/updated-final_biologicals-and-inno.pdf


  4. Guideline For Good Regulatory Oversight of Clinical Trials(2022) central Administration For of biological products & clinical trials,available at https://www.edaegypt.gov.eg/media/jsgcbt4i/guideline-for-good-regulatory-oversight-of-clinical-trials-by-egyptian-drug-authority-1.pdf


  5. List of Essential required documents in the file of the investigator and/or sponsor/CRO to be submitted to EDA for clinical trials to be conducted in Egypt (2022) central Administration For of biological products & clinical trials,available at https://www.edaegypt.gov.eg/media/fbmb5irv/list-of-essential-required-documents-for-clin_biologicals-and-inno.pdf


  6. GUIDELINE ON Administrative requirements for variation submission of Biological Products(2022) central Administration For of biological products & clinical trials,available at https://www.edaegypt.gov.eg/media/cesfvrnj/administrative-requirements-for-variation-submission.pdf


  7. Applicant request to the Egyptian Drug Authority For Clinical Trial Authorization on a medicinal product for Human use (2022) central Administration For of biological products & clinical trials,available at https://www.edaegypt.gov.eg/media/ps5plrvo/2-application-form-applicant-request-to-the-egyptian-drug-authority-for-clinical-trial-authorization-on-a-medicinal-product-for-human-use.pdf


  8. Medical-device-registration-egypt (2022), Available at: https://operonstrategist.com/medical-device-registration-egypt/
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