.

Mission:

 Become global service oriented CRO (Contract Research

Organization) in the pharmaceutical field.
 Deliver fast top quality data, at competitive prices.
 Ensure absolute comfort and safety of our citizens.

3. Quality Policy:

 We seek to meet and exceed expectations on the basis of quality

international top clinical practices.
 Our team is experienced and well trained.
 Our in house S.O.P.s are developed to ensure that our procedures,
system, and associated documentation and controls comply with
regulatory MOPH guidelines.

4. Organization:

• General Manager: Dr. Dina Wahba.

• Technical Manager: Dr. May Amin.
• Quality Assurance Manager: Ch. Ayatollah Mohamed Badr.
• Clinical Investigator: Dr. Abdel Wahab Mohamed.
• Study Coordinator: Dr. Asmaa Elrayess.
• Chief Analyst.
• Analysis Staff: Dr. Ahmed Yehia.
• Administration Staff.

• Physician: MSA BE Center has a Physician (Internal medicine), who

is specialized for physical examination of the volunteers, observing them
during taking the samples and also observes any side effects or adverse
events.
• Nurse: specialized for sampling and plasma separation.
• Technician: help nurse to perform their work.
• Study Coordinator: prepare randomization plan and supervise the
process of study coding.
• Cleaning Staff: keeping place clean and healthy.
5. Facilities:

1. Reception
2. Administration Room
3. Archiving Room
4. Drug Samples Store
5. Chemical Store
6. Staff Dining Room
7. Staff W.Cs
8. Instrumental Lab.
9. Data Processing Room
10. Preparation Lab.
11. Subject Housing Room: provided with 40 beds and 40 lockers for
volunteers.
12. Samples withdrawal Room: well equipped for sampling withdrawal
with centrifuge and deep freezer (-80◦ C).
13. Physician Room: well-equipped physician room with examination
bed and blood pressure monitor. All first aid medications are kept in the
first aid locker and oxygen cylinder.
14. Volunteer Dining Room: full facilities to prepare study meals.
15. Volunteer W.Cs.

6. Services:
1. Bioequivalence & Bioavailability studies
2. Bio-analytical services
3. Method development from scratches
4. Fine tuning of existing methods
5. Method validation according to validation protocol
6. Bio-waiver and comparative in-vitro dissolution studies
7. Formation studies
8. Training service
9. Research projects