Chandigarh, Chandigarh, India
$5/hr · Starting at $25
Holding 15 years experience in Regulatory Affairs API. Hands on Sterility Assurance package to be used in DMF. DMF submission across the globe USDMF, ASMF, CEP. Expert in ICH guidelines.
Palm Beach Gardens, Florida, United States
$90/hr · Starting at $25
Quality, Regulatory Affairs and Compliance Consultant for the medical device, life science, fields..
Hoover, Alabama, United States
Masters in Regulatory Affairs from Johns Hopkins with internship experience at Pfizer and have clinical regulatory experience from an academic institute
Miami, Florida, United States
$50/hr · Starting at $25
The services I can assist with include: PRE-MARKET RELATED POST-MARKET RELATED GENERAL REGULATORY AFFAIRS - Regulatory project management - Regulatory/Compliance strategy development - Workshops and
Bengaluru, Karnataka, India
$10/hr · Starting at $30
Consultancy for Preparation of Technical File, CE Marking and product registration into different countries with testing of products through test labs.
Mumbai, Maharashtra, India
$10/hr · Starting at $90
I am into Regulatory Affairs since 3 years. Following are the services :- 1) Dossier preparation as per different country's guidelines. 2) CTD format dossier preparation 3) Dealing and resolving dif…
Lagos, Lagos, Nigeria
Filing of application to FDA in anglophone west Africa countries. CTD dossier review, Gap analysis, product lifecycle maintenance, labeling . Artwork design. Clinical trials filings.
Cluj-Napoca, Cluj, Romania
$30/hr · Starting at $50
Pharmacist with knowledge in Regulatory Affairs field, Medical Writing and Pharmacovigilance. Experienced in Drug Product Submissions (compillation of dossiers), CL,eAF,SmPC,PL management SOP review
$40/hr · Starting at $30
I had an extensive Pharmaceutical industrial experience in Regulatory Affairs Department as Manager. In addition I worked as Pharmaceutical lecturer and taught B.Pharm and M.Pharm students and took bo…
Hyderabad, Telangana, India
$15/hr · Starting at $30
Expertise in Pharma Regulatory intelligence which involves research on the latest regulatory updates
$80/hr · Starting at $100
I am experienced in labeling for US market. Including PIL, draft container and carton labeling text, side by side comparison. Expert in making SPL.
Zagreb, Grad Zagreb, Croatia
$50/hr · Starting at $200
RA services, knowledge of national regulations related to medicinal products, medical devices, cosmetics, food supplements, excellent English - Croatian knowledge for these specific product categories…
Ahmedabad, Gujarat, India
Drug regulatory affair professional with expertise in - 1.Dossier compilation for registration of drug product for global market. 2.Countries/region for which services provided - a. India…
Ben Aknoun, Alger, Algeria
$25/hr · Starting at $25
I am a regulatory affairs pharmacist with more than 8 years experience in regulatory affairs. Having a good knowledge of the local pharma environment, I can support and represent companies in Algeria
Angamaly, Kerala, India
$100/hr · Starting at $50
Medical writing, Medicines submission to EMA & FDA, eCTD, CMC writing, Labelling, GCC, Clinical overview, PSUR, Module 3, dossier compilation, DCP, Scientific Advice, Dossier Audit
Christiana, Delaware, United States
$125/hr · Starting at $25
A highly proficient Medical Devices professional and a leader with variety of skill sets in Quality assurance and Regulatory Affairs. I have over 10+ years of experience working for Fortune 500 compan…
Vadodara, Gujarat, India
$40/hr · Starting at $100
Technical file preparation and review of medical device as per EUMDR 2017/745, gap assessment of QMS documents, QMS documents preparation and review for ISO 13485, 510k dossier preparation and review
$15/hr · Starting at $25
I have more than 8 years of experience in Pharmaceutical Industry. • Compilation and preparation of a high quality CTD dossier as per specific country requirements. • Collecting, collating and evalua…
Zichron Y'aakov, HaZafon, Israel
$100/hr · Starting at $100
am a regulatory affairs consultant in Israel. I can prepare submissions to the Israeli Ministry of health in a professional manner. I worked for a global medical device company for 13 years(Covidien n…
San Jose, California, United States
Over 15 years of experience in R&D, regulatory, quality assurance and compliance. Strength lies in GLP, QC, QA, pre-IND, IND, CTA , BLA, 510 (k) submissions, compliance, training and auditing, grant…