Profile Summary
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
A dedicated Regulatory Affairs and Quality Assurance professional (Medical Devices) having 3.4 years of experience in US FDA, EU MDD, and ISO 1...
Pharmaceutical Regulatory Affairs professional with more than 10+ years in industry experience in Formulations.
Lakshmi K.
Pharmacologist, 5 years experience in Analytical and Bioanalytical, Can write Standard operating procedures, Reports. Perform literature search...
Tasmiatul K.
1. Registered and Licensed Pharmacist (RPh) in Bangladesh (Reg. No- A 4845) 2. Experienced Professional equipped with skills in the field of Re...
Anne Betty graduated with a bachelor’s honours degree in Biomedical Sciences from the University of Bradford; and is both a Registered Nutritio...
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Coordinated multiple number of regulatory and pharmacovigilance projects such as finalizing regulatory strategy roadmap, technical review of co...
MIRZA WAJID B.
11 years' experience in Quality, Health and Safety, Food Safety, HACCP, Hygiene as well as Internal Auditing/External Supplier Auditing in ...
Vandita S.
Expertise in Development of innovative, green & cost effective products & processes for Nutraceuticals, Dietary supplements, Cosmetic...
I am quick, thorough, and will exceed your expectations. A professional with 12+ years of experience in academic, scientific, technical, and co...
Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...
I am a chemical engineer with experience in product development, product formulation and production managment. I already worked in different in...
I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...
Vandana C.
Experienced leader with a demonstrated history of global project management in the CRO with over 9 yrs of successful experience in Regulatory S...
PROFESSIONAL PROFILE: A Regulatory Affairs/ Quality Operations Professional with thirteen years drug development experience (Pharmaceutical), w...
- Skilled in QMS ISO 13485/9001, ISO 14971, 21 CFR Part 820, MDD 93/42/EEC & MDR 2017/745. - Highly experienced in Balloon Catheter, St...
Roselyn B.
Food Technologist specializes in Product Development and Regulatory Documentations
Muhammad H.
I am a certified Data Analysis professional, I possess extensive hands-on experience with Microsoft Power BI, DAX and Tableau, enabling me to d...
20 years in Medical Devices, QA. RA, Validation for all Classifications of Medical Devices. MDR. IVDR expertise, with Software as a Medical Dev...
Prerana D.
A clinical research post-graduate having a vast knowledge over a range of Medical devices consulting services on conformation of 62304:2006 sta...
Dr. Loleta R.
Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...
CAREER SUMARY • 33 Years of broad working experience having worked with different Pharmaceutical, Biopharmaceutical and Vaccine manufacturers ...
Materials scientist with specialization in plastics design, analysis, processing and longevity, particularly in medical plastics and birth cont...
We would like to take this opportunity to introduce our organization- Let’s Evolve Life that specializes in Clinical trial/study design service...
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