San Jose, California, United States
$50/hr · Starting at $25
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…
Mumbai, Maharashtra, India
$5/hr · Starting at $25
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.
Orlando, Florida, United States
$80/hr · Starting at $40
Joanne Northcutt, PhD is a regulatory and medical writer with over 15 years of experience in pharmaceutical Phase I-IV clinical trials. Services: Write, edit, and review fully ICH-compliant regulator…
Kolkata, West Bengal, India
Drafting, Conveyancing, Advisory, Para legal, Litigation Management, Liasioning, Compliance and Licenses, Legal Audit, Template Formulation, Contract Management and Para Legal
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…
$15/hr · Starting at $25
With over 6 years experience I am the perfect freelancer to complete your tasks. I am reliable, I take my work seriously and I deliver it on time in order to meet TAT and SLA. ?My key skills are in le…
Lahore, Punjab, Pakistan
ID Verified
$25/hr · Starting at $100
Regulatory compliance and reporting needs are to be viewed as a natural extension of the governance issues to be handled by top management and corporate Boards. It can ensure that compliance is aligne…
Hyderabad, Telangana, India
$15/hr · Starting at $30
1. Clinical Regulatory Services Clinical Trial Submissions Clinical Study Design Sample Size Estimation Protocol Synopsis Protocol Development Informed Consent Form Advertising Material Insurance and
Mississauga, Ontario, Canada
$75/hr · Starting at $25
We can assist you through the product certification process. We have worked extensively with the IEC61010 and IEC60950 product safety standards. Working partners include CSA, ESA, Entela, and Lamothe
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…
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…
Jersey City, New Jersey, United States
$35/hr · Starting at $35
Have a question about FIRRMA and the CFIUS review process? Let me do some research and find out for you. I have spent about 80 hours researching and summarizing these areas. I can provide informal
Albany, Oregon, United States
$100/hr · Starting at $500
I have 15 years experience with Hewlett Packard and 4 years with Polycom as a International Compliance Manager. I can deal with agencies, test houses, OEM's and vendors to get your ITE, A/V and light…
$20/hr · Starting at $25
A B. Tech Mechanical Engineer offering 6 years of product-development & designing solutions in Medical Devices products. Notable Clients for which product development-engineering services were offered…
Philadelphia, Pennsylvania, United States
$20/hr · Starting at $100
Phd in Biochemistry. Published fifteen scientific original research articles and two book chapters. Scientific blog writer
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…
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
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…
Irving, Texas, United States
$250/hr · Starting at $250
I bring the wide-ranging experience of 18 years of all aspects of the food industry, from the microbiology of safe food preservation to the exploration of new food markets to legal compliance issues w…
Ashburn, Virginia, United States
$195/hr · Starting at $25
Design and build, develop, enhance, support, or evaluate regulatory trade program covering export control, economic sanctions, modern slavery, data privacy protection, anti-bribery and corruption, ant…