Eden Prairie, Minnesota, United States
$50/hr · Starting at $35
Provide strategic and tactical direction for all regulatory, clinical, product safety, design, registration and post-market surveillance activities. Provide regulatory assistance on medical devices, O…
Fort Wright, Kentucky, United States
$150/hr · Starting at $100
I provide complete support from preparing initial pre-IND packages and FDA meetings, to developing all modules of the IND for submission. I can support you as you develop your NDA or BLA to bring a dr…
Campinas, Sao Paulo, Brazil
$200/hr · Starting at $25
The regulatory process from product design to market entry for a new medical device or IVD is oftentimes complicated and unclear. In Brazil, it can also become difficult to make a clear distinction be…
Pune, Maharashtra, India
$9/hr · Starting at $50
Provide End to end regulatory solutions as below: US/EU - Submissions in CTD/eCTD format with Due diligence and compilation Asian submissions Indian submission Other countries product registrations.
Bengaluru, Karnataka, India
$5/hr · Starting at $25
Siddharth Gupta is a Chartered Accountant and a law graduate. He has over 10 years of experience in the tax and regulatory space. He has represented clients before the regulatory authorities at variou…
Chicago, Illinois, United States
$40/hr · Starting at $25
I am an independent regulatory consultant who works with manufacturers to ensure the compliance of company documents with the latest regulations at the state and federal level. To date, my experience
Vilnius, Vilnius, Lithuania
$25/hr · Starting at $50
Anton Sudnik can help you with all regulatory and compliance issues. Anton will ensure that your business is in compliance with all necessary regulations and standards. The Regulatory Compliance Advis…
$10/hr · Starting at $30
Quality and Regulatory consultant for medical devices , support in creating DHF file , Preparation of Risk Management plan , Preparation of hazard analysis , FMEA ,Reviewing User manuals , Technical f…
Mumbai, Maharashtra, India
$10/hr · Starting at $90
I am into Regulatory Affairs since 3 years. Following are the services :- 1) Dossier preparation as per different country's guidelines. 2) CTD format dossier preparation 3) Dealing and resolving dif…
Kilkenny, Kilkenny, Ireland
Accountancy professional with experience preparing monthly management accounts and cash flows, board reporting. Highly experienced in the preparation of financial statements and managing audits. Most
Kazhakkoottam, Kerala, India
$15/hr · Starting at $25
Experienced regulatory document publisher and medical writing quality reviewer. Tasks Familiar: Document publishing(All clinical documents) Quality check(All clinical documents) Data entry,PDF merging…
Yerevan, Yerevan, Armenia
$20/hr · Starting at $30
Regulatory Compliance Officer specialized in Business Consulting, International Regulations, Contracts, Agreements, Policies, GDPR/ CCPA/DPA, AML & KYC, PSD2. I have around 8 years of experience in th…
South Haven, Michigan, United States
$100/hr · Starting at $100
I have significant experience as a Human Resources Director, Healthcare Director and in regulatory compliance. I will apply these skills to help care for your business.
New Delhi, Delhi, India
$15/hr · Starting at $50
We provide end to end taxation and regulatory services to clients from various spectrum.Our services include : Direct and GST litigation, consultancy and compliance services( e.g return filing ) Busin…
East Haven, Connecticut, United States
I am a highly experienced editorial professional and subject matter expert in human resources and environmental, health, and safety regulatory compliance and training requirements. My accomplishments
Denver, Colorado, United States
Co-founder of www.complect.co where businesses can come to find financial regulatory compliance specialists on demand. All specialists have a minimum 3 year direct work experience in the space. We are…
Delhi, Delhi, India
I will write articles or regulatory medical modules specifically module 4 and module 5. I have well experienced in pharmaceutical company as medical writer but I am new on freelancing so give me the c…
Christiana, Delaware, United States
$125/hr · Starting at $25
A highly proficient Medical Devices professional and a leader with variety of skill sets in Quality assurance and Regulatory Affairs. I have over 10+ years of experience working for Fortune 500 compan…
Mississauga, Ontario, Canada
$100/hr · Starting at $300
I provide a wide range of technical expertise in relation to toxicology and regulatory compliance. I am a board-certified toxicologist (DABT), with over 15 years of experience helping companies in the…
Lagos, Lagos, Nigeria
Filing of application to FDA in anglophone west Africa countries. CTD dossier review, Gap analysis, product lifecycle maintenance, labeling . Artwork design. Clinical trials filings.