Profile Summary
Shiraz A.
Medical writer with experience in FDA/PAAB compliant promotional assets for HCP, Patient, and DTC audiences. Proficient in MLR submissions and...
Rachid E.
My qualification is an MSc in Biomedical Sciences. I am a Regulatory Affairs Specialist. The primary responsibilities are: - Working with CTD ...
Priyanka W.
Experience in following: - Clinical Operations: Clinical Monitoring, Therapeutic Areas, Clinical Trial technologies, QMS Management - People M...
Reema D.
• Preparation of CTD sections of the dossiers required for Regulatory submission in various countries namely EU (National, MRP and DCP), US (AN...
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Sukanya C.
• Proficient at downstream process development activities, experimental design and execution for viral vector and other drug substance purifica...
Nidhi S.
Expert in development of new products and new process technologies for both pharmaceutical and nutraceutical solid dosage forms especially oral...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
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Janita ..
I am a result-oriented professional with 8+ years of experience spanning across academic, research, and industry. I am qualified as a Master of...
Jessica B.
Global Project Leader in Psychiatry & Neurology. Former Research Scientist in Psychiatry. Experienced ACRP Certified Clinical Research Coor...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
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Hiring for pharmaceutical regulatory affairs consulting services$500.00
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