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.
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…
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
$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…
Kolkata, West Bengal, India
Drafting, Conveyancing, Advisory, Para legal, Litigation Management, Liasioning, Compliance and Licenses, Legal Audit, Template Formulation, Contract Management and Para Legal
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
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
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…
$30/hr · Starting at $500
Compliance and regulatory support services assist organizations in meeting industry regulations (e.g., GDPR, HIPAA) and compliance requirements related to cybersecurity. Leveraging my expertise in reg…
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
Bengaluru, Karnataka, India
$30/hr · Starting at $350
Category: Consulting → Financial Consulting Description: Need help meeting a financial reporting deadline? I provide expert support in regulatory compliance, schedule preparation, variance analysis, a…
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
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…
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…
Lonndon, England, United Kingdom
$350/hr · Starting at $2,500
Trellis Fi provides regulatory compliance, AML CFT & verification services to help clients meet their obligations through access to global sanctions screening and connectivity with all important lists…