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Personal Information
Organization / Workplace
Ahmedabad Area, India, Gujarat India
Occupation
Research Associate - Bioanalytical Department at Veeda Clinical Research
Industry
Medical / Health Care / Pharmaceuticals
About
Highly energetic, task oriented pharmaceutical professional with keen knowledge in regulatory affairs and actively seeking for job oppertunities in Regulatory Affairs in Pharma/Biotech Companies around Ahmedabad. I have completed B.Pharm from L. J. Institute of Pharmacy and cleared my M.Pharm (Quality Assurance and Pharm Regulatory Affairs) from the same, L. J. Institute of Pharmacy with Distinction. I am now seeking for job as Regulatory affairs professional. I am a self-motivated, proactive individual with profound knowledge in Regulatory Affairs. Clinical Research and Quality Assurance for drugs, biologics and medical devices. I have a voracious capacity to learn new concepts, have t...
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Documents(15)Ìý

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Preparation of Clinical Trial Protocol of India.
Preparation of Clinical Trial Protocol of India.Preparation of Clinical Trial Protocol of India.
Preparation of Clinical Trial Protocol of India.
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To prepare & compare Label, prescribing Information & Patient Information leaflet of REYATAZ (Hard Gelatin Capsule)
To prepare & compare Label, prescribing Information & Patient Information leaflet of REYATAZ (Hard Gelatin Capsule)To prepare & compare Label, prescribing Information & Patient Information leaflet of REYATAZ (Hard Gelatin Capsule)
To prepare & compare Label, prescribing Information & Patient Information leaflet of REYATAZ (Hard Gelatin Capsule)
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To compare filing process of NDA of different countries of India, US and Europe. B) Preparation of global list documents of registration of IND and NDA as per USFDA and Europe.
To compare filing process of NDA of different countries of India, US and Europe. B) Preparation of global list documents of registration of IND and NDA as per USFDA and Europe.To compare filing process of NDA of different countries of India, US and Europe. B) Preparation of global list documents of registration of IND and NDA as per USFDA and Europe.
To compare filing process of NDA of different countries of India, US and Europe. B) Preparation of global list documents of registration of IND and NDA as per USFDA and Europe.
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