Spring Hill, Florida, United States
$5/hr · Starting at $25
CONTACT US FOR PRICING - With our in-depth expertise, we can assist with mitigating organizational risk, ensuring workforce management policies and practices are compliant with complex and regularly-c…
Daytona Beach, Florida, United States
$225/hr · Starting at $25
I have several years experience on Wall Street and as a consultant working with registered investment advisors and broker dealers. Not only can I help advisors prepare for SEC, FINRA, and state regula…
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.
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
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…
Cairo, Al Qahirah, Egypt
$50/hr · Starting at $50
Product compliance, Regulatory advices, Label preparation and proofread( Arabic, English, French), Registration dossiers preparation ( food, fortified food, food supplements, Halal), Health and nutrit…
Sheridan, Wyoming, United States
Experienced Quality Assurance Consultant with a demonstrated history of working in Medical devices, Drugs, Biologics, and Combination products. Skilled in Regulatory Affairs, Quality Assurance, Clinic…
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
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
Houston, Texas, United States
Offering startups and existing businesses regulatory compliance services and solutions in the financial services and cannabis industry. Experienced Compliance professional with a demonstrated history
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…
Bhopal, Madhya Pradesh, India
$40/hr · Starting at $80
Navigate complex regulatory landscapes with confidence. My expertise covers Factory Act compliance, Environmental clearances (PCB), Labor Law compliance (ESIC, PF), and international standards (API 65…
Nairobi, Nairobi Area, Kenya
$10/hr · Starting at $50
Regulatory Compliance Officer specializing in compliance risk identification and management, Anti Money Laundering, KYC, Enhanced Due Diligence, and Training. I have over 10 years of experience in th…
Long Beach, California, United States
$125/hr · Starting at $1,000
An accomplished professional with a proven track record developing effective risk management and regulatory compliance programs in the healthcare industry Specialties: FDA, HIPAA, CCPA and GDPR data p…
Pimpri, Pune, Maharashtra, India
ID Verified
$15/hr · Starting at $150
I provide the medical devices consulting by providing the services for CE marking, 510 k, ISO 13485, 21 CFR part 820 implementation, Medical devices manufacturing unit design, Design and development d…
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…
$20/hr · Starting at $25
Compliance professional with more than 7 years of expertise in vendor due diligence, third-party risk management, anti-money laundering (AML), and sanctions. Strong writing, critical thinking, researc…
Guangzhou, North-West Frontier, Pakistan
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…
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…
Mumbai, Maharashtra, India
$30/hr · Starting at $60
I am Youngest Expertise In regulatory Pharmaceuticals, Still Learning and working though. Yet I can provide you best guidance in this field. I can Help you 1. Registering product 2. Site Regestration…