Services

BIOMISR

is a technical consulting company in the field
of pharmaceutical industry
GMP consultation in the field of
pharmaceutical, food, medical and health
care industry.
Exportation of all pharmaceutical products
through delegation from the producers

Finalize all the documents and licensing needed
in pharmaceutical industry at the Egyptian
Ministry of Health

Including:

Civil structure, architecture, power and
Electro-mechanical engineering studies according
to GMP guidelines

Registration of pharmaceutical, food, and
medical products.

APIs Supplier

Exportation of all pharmaceutical products
through delegation from the producers

Provides comprehensive pharmaceutical soultion in the Egyptian market. Our experts team play an important role in supporting our clients in various fields in pharmaceutical industry including registration ,production and marketing

Total solution for the entire process of regestration and production of pharmaceutical products, food supplement, cosmetics ,and medical device.

Marketing research services for new products and consultation services for pharmaceutical factories including layout, HVAC, GMP, GSP, GLP

Training service in all pharmaceutical fields including pharmacovigilance,bioequevalence, registration ,CTD,eCTD,—–

Marketing Research

Biomisr provide data analysis for a selected pharmaceutical market, forecasting of sales of a particular drug or medical device in the selected time horizon before entering the market.

Pharmacovigilance Services

BioMisr group has its own in-house pharmacovigilance system.

BioMisr provide pharmacovigilance services as an outsourcing partner for other pharmaceutical companies

Training Services

GMP
QUALITY IN ACTION
QMS
HVAC
BIOEQUAVALENCE
PHARMACOVIGILANCE
RISK ASSESSMENT AND SCIENTIFIC PROBLEM SOLVING

Technical consultations

Provide technical support in plant design according to GMP requirements.
Development of Standard Operating Procedures (SOPs)  PlanningandinstallationofGMP-compliantQAsystems  CriticalreviewandoptimizationofQAsystems
Validationmasterplan–Qualificationofequipment–Process validationandMethodvalidation
Planningandconductofmock-inspections and preparation of inspection reports
PharmaceuticalIngredients(APIs)
Set up of quality management system

Regulatory affairs activities

1-Rregistration of all pharmaceuticals in a comprehensive work file CTD , and eCTD.
2- Carry out Bioequivalence studies at GCC accredited center
3-Provide professional pharmacovigilance files
4- Stability studies
5- Bioequivelance studies

Pharma consultation

GMP consultation in the field of:
Pharmaceutical.
Food.
Medical and health care industry.