Singapore, Singapore, Singapore
$70/hr · Starting at $50
Armed with 8 years of experience in the healthcare industry, I am equipped for dealing in all kind of regulatory operations support (off site), regulatory product submission, commercial sourcing and a…
Shepherdstown, West Virginia, United States
$100/hr · Starting at $300
Services Offered Regulatory Compliance FIFRA pathway assessments, EPA submission reviews, state registration strategy, deficiency letter responses, and regulatory due diligence for investors. Grant W…
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.
Hyderabad, Telangana, India
$10/hr · Starting at $25
1) expertise on regulatory fillings to USFDA and DCGI(CDSCO, SUGAM, NDPS, CBN). 2) expertise on ICH and Drugs and cosmetics acts and Narcotics act
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
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.
Buenos Aires, Buenos Aires, Argentina
$200/hr · Starting at $200
I'm helping companies to authorize and launch products globally, in the following key areas: Registration process for Cosmetics, Medical Devices, OTC, IVD and Food to FDA approval process, INVIMA (Col…
Cincinnati, Ohio, United States
$30/hr · Starting at $25
Graduate of Xavier University with a Bachelor in Science. I have been working in the Clinical Research Industry for 5 years now. I have worked for both the private and public sector. I spent 3 years w…
Guangzhou, North-West Frontier, Pakistan
ID Verified
$40/hr · Starting at $100
I offer full service by providing guidelines for submission of generics (ANDA) to the FDA, EMA, and MHRA. Dossiers drafting, review, and submission via ECTD to avoid RTR (refuse to review). Formatting…
Sahibzada Ajit Singh Nagar, Punjab, India
$20/hr · Starting at $50
Single step consultancy for all regulatory services. CDSCO filings & approvals Design/development & assistance in the preparation of Common Technical Documents (CTDs). Medical Devices Registration. Cr…
Nairobi, Nairobi Area, Kenya
$120/hr · Starting at $110
Provide comprehensive Regulatory services across the spectrum of global product development, registration and commercialization. Specializes in Dossier strategy, Dossier Gap Analysis, Dossier Compilat…
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…
Gurugram, Haryana, India
Areas of Responsibility: • Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies • Evaluates the regulatory environ…
Lahore, Punjab, Pakistan
$8/hr · Starting at $25
If you are dealing chemicals for import or export business and in need of Material safety data sheets based on the composition info for the product provided and classified according to the Globally Ha…
Airdale Close, England, United Kingdom
$45/hr · Starting at $200
I am a doctor working in the NHS in the UK. I have developed several guidelines, how-to's, health policies and policies in the field of medicine and health. These include - the health section of an ai…
Wilmington, Delaware, United States
With opportunity, comes regulation and documentation. I have developed cannabis industry Standard Operating Procedures and Business Operations Plan templates that have proven successful in allowing my…
Lorton, Virginia, United States
$25/hr · Starting at $250
I am a highly-motivated, honest and reliable Information Technology Manager and Cyber Security Professional, that specializes in information security architecture, configuration / change management, c…
Gurgaon, Haryana, India
I currently working Healthcare MNC Organization. Being an start up organization i am taking care of multiple task i.e. Quality assurance, Regulatory operation, Data Entry , Document Control and Market…
Ahmedabad, Gujarat, India
A medical doctor, trained in anaesthesiology has a good knowledge of drug development drug safety and regulatory process.
Bangalore, Karnataka, India
Hands on experience in Safety Data Collection, Safety Data entry, Safety Case Review, MedDRA coding,WHO Drug Coding and various reports generation e.g. PSUR, DSUR, CIOMS, MedWatch e.t.c. Expert in pre…