Lagos, Lagos, Nigeria
$5/hr · Starting at $25
Filing of application to FDA in anglophone west Africa countries. CTD dossier review, Gap analysis, product lifecycle maintenance, labeling . Artwork design. Clinical trials filings.
Tempe, Arizona, United States
$25/hr · Starting at $25
Retail Rate Design Real-Time Pricing Purchase Power Agreements Regulatory Compliance Marginal Cost Methods FERC Form-1, SEC 10-K, FCC Forms 499-A, 499-Q Budget Variance Analysis spreadsheets Functi…
Hyderabad, Telangana, India
$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.
Abidjan, Abidjan, Ivory Coast
$20/hr · Starting at $500
can help your for registration and renewal or marketing Authorization into all french Speaking Africa.
Lafayette, Colorado, United States
Review product / project to make sure it is in compliance with all standards and regulatory requirements - Review product / project - Create list of regulatory / standards requirements - Review list o…
$25/hr · Starting at $500
Can prepare and review. documents for Europe dossier submission as per EU guidelines.Can prepare CCDS documents, RMP, xEVMPD submissions. Can file variations, line extensions, repeatuse procedures, re…
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
$10/hr · Starting at $30
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…
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…
Kishangarh, Rajasthan, India
$10/hr · Starting at $25
Accounting and Finance | Regulatory & Compliance | Big Data Processing | Trademark and Registration | Insurance Advisory | Labor Act and Factory Establishment Compliance | Startup Marketing and Press
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.
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…
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…
Kolkata, West Bengal, India
Drafting, Conveyancing, Advisory, Para legal, Litigation Management, Liasioning, Compliance and Licenses, Legal Audit, Template Formulation, Contract Management and Para Legal
$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…
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
$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
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…