Afra Pharma Consultant is a leading provider of quality resources for the regulation of pharmaceutical products, including consumer health and over-the-counter medications. Established in 2011, Afra Pharma Consultant serves a global network of clients across Europe, Asia, North Africa, the GCC region, Saudi Arabia, and India. Located primarily in Pune, India, Afra Pharma Consultant is dedicated to meeting the latest regulations and stringent requirements of the pharmaceutical industry.
Afra Pharma Consultant offers a comprehensive range of services, including training, PIL (Patient Information Leaflet) support, project management, audits and inspections, and strategic planning. These services are tailored to meet the individual requirements of pharmaceutical companies of all sizes. Afra Pharma Consultant is committed to supporting pharmaceutical manufacturers with dossier support, clinical trials, and technology transfer initiatives.
Afra Pharma Consultant strives to develop long-term relationships with clients based on integrity, professionalism, and trust. The company is committed to conducting business ethically and in a socially responsible manner, ensuring excellence in pharmaceutical consultancy services.
The primary address for Afra Pharma Consultant is Pune, IN. We invite the management team at Afra Pharma Consultant to create a customized and exclusive company showcase and product listing on our platform.
Compare Afra Pharma consultant with 1 companies in Pharmaceutical-Manufacturing
| Comparison Field |
Afra Pharma consultantMain Company |
ONIX Life Sciences L...View Profile |
|---|---|---|
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Founded Year
|
— | 2010 |
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Company Size
|
— | 2-10 |
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City
|
Windsor, Berkshire | |
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Country
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United Kingdom | |
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Skills & Keywords
Comparing with main company
|
19 Total Skills
Pharmaceutical Regulations
Regulatory Affairs
Pharmaceutical Manufacturing
Dossier Support
Clinical Trials
Audits and Inspections
Strategic Planning
Regulatory Support
GCC
Sourcing Contract manufacturing.
eCTD)
Exports & tenders
eCTD
Clinical Trails
Sourcing Technology transfer & joint ventures.
BA/BE Studies from approved US FDA & GCC CROs.
Dossier Support (US
EU
CTD
|
22 Total
1 Common
21 Unique
Match
5%
Common Skills:
Regulatory Affairs
Unique Skills:
ASMF
BLA
CmDh
CTA
CTD MS Word Templates
DMF
+15
|
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