Golden Valley, Minnesota, United States
$75/hr · Starting at $50
Jonathan Lendrum is an experienced, business-minded Regulatory Professional for the Medical Device Industry. Combining his experience as a researcher and regulatory affairs and quality assurance consu…
Centro, Montevideo, Uruguay
$5/hr · Starting at $50
Asistencia al área regulatoria y trato con proveedores para empresas dedicadas a la venta y distribución de equipamiento médico, experiencia en formular los expedientes, contacto con los diversos prov…
Dhaka, Dhaka, Bangladesh
$5/hr · Starting at $25
Dear concern, I would like to let you know that I’m a very hardworking and dedicated person. I only take payment when my clients smiles on my output. I’ll do my work with full honesty. As I am a new f…
Cairo, Al Qahirah, Egypt
$70/hr · Starting at $300
Regulatory Affairs/Intelligence (Pharma/Consumer Health/MD)-(MEA/LEVANT/APAC/CIS/Others). Regulatory End to End consultation service. I am working in the field of Pharmaceutical Industries; I am a pha…
Malakand, 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…
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…
New-Delhi, Delhi, India
$50/hr · Starting at $1,000
Global Regulatory & Consumer Insights have a wealth of technical and practical experience in regulatory affairs, pharmacovigilance, licensing and strategic development, and can offer advice, guidance
new delhi, Delhi, India
$20/hr · Starting at $25
I have a bachelor’s degree in industrial microbiology and master’s degree in toxicology with 3 years of experience working as an Senior-executive regulatory affairs as a toxicity expert where I gained…
Dubai, Dubai, United Arab Emirates
$20/hr · Starting at $200
Sector : FMCG, Biotech, Health My scope: Market research, Export/Import, regulatory watch, path to market support for the international companies such as Gilead, RB, C&D, JnJ, L´Oreal, etc.
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…
Abu Dhabi, Abu Dhabi, United Arab Emirates
Carrying out Seminars and Lectures on different Regulatory affairs subjects and issues and the latest ICH quality guidelines.
Gurugram, Haryana, India
$10/hr · Starting at $25
Areas of Responsibility: • Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies • Evaluates the regulatory environ…
Oak Park, Illinois, United States
$200/hr · Starting at $1,000
At Dillard & King, our Government Affairs Practice Group is dedicated to providing strategic guidance and advocacy on matters relating to government relations, policy, and regulatory affairs. We under…
Collierville, Tennessee, United States
We have 20+ years of experience in the medical device and pharmaceutical regulatory consulting arena. We provide assistance with health registration dossiers, design dossiers, technical files, CE mar…
Sumare, Sao Paulo, Brazil
$60/hr · Starting at $300
JS Consulting is a company specialized in providing COMPANY PROFILE Our Services : Sanitary Licensing With hundreds of successful cases since its founding in 2006, the Working in partnership with our
Abidjan, Abidjan, Ivory Coast
$20/hr · Starting at $500
can help your for registration and renewal or marketing Authorization into all french Speaking Africa.
Mumbai, Maharashtra, India
A professional having 10 years of experience for dossier preparation in EU, South Africa, Australia, WHO and ROW market. Expert in dossier authoring, variation package and other LCM submission.
Surat, Gujarat, India
$25/hr · Starting at $25
Professional Summary Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in medical device review and evaluation. Superb multitasker able to handle m…
Karachi, Sindh, Pakistan
$30/hr · Starting at $30
Do you need assistance with CTD dossier preparation? Do you wish that your products comply with the local and export criteria along with DRAP Regulations? Is the complexity of document preparation for…
Bhavnagar, Gujarat, India
$8/hr · Starting at $25
Regulatory Affairs Services includes DMF, ASMF, CQA, ICH, USFDA, MCH and DCGI Documentation etc.Genuine and Transparent Service