AHMEDABAD, Gujarat, India
$8/hr · Starting at $25
4+ Year of experience in Pharmaceutical Industry Includes, 1. Preparation of DOSSIER for all pharmaceutical Products 2. NDA, ANDA filling, e-CTD 3. Sourcing of Pharmaceutica…
Beograd, Serbia, Serbia
$20/hr · Starting at $50
Translation of pharmaceutical documentation for regulatory purposes (Summary of Products Characteristics (SmPC), Patient Information Leaflet (PIL), clinical protocols, case report forms, CTD, PSUR, in…
Sahibzada Ajit Singh Nagar, Punjab, India
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…
Ghaziabad, Uttar Pradesh, India
$80/hr · Starting at $3,200
Registered pharmacist with 12+ years of Regulatory and commerical medical writing experience in the pharmaceutical industry. I have experience in writing and managing the common technical documents (C…
Vettichira, Kerala, India
$10/hr · Starting at $25
I am a Mechanical engineering graduate specialized in MEP Design and supervision. I have completed Diploma in MEP under CTDS Certification. I have working experience for a private MEP Consultancy name…
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…
Lahore, Punjab, Pakistan
$10/hr · Starting at $30
I have done a graduate degree in Pharmaceutical Sciences and has been working for over 2 years in the R&D department of a Pharmaceutical Industry. I am also going through post graduation these days an…
Kolkata, West Bengal, India
$8/hr · Starting at $32
Skill Set STLC Model:- Methods: Black Box testing, White box Testing, Gery Box Testing Levels: Functional Testing, Unit Testing, Integration Testing, System Testing, Regression Testing Documen…
Bengaluru, Karnataka, India
I am a post graduate with 2 years of experience in medical writing. I have been writing clinical, regulatory, and scientific documents. I can help you in poster designing, manuscript writing, copy wri…
Guangzhou, Guangdong, China
$40/hr · Starting at $100
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…
Gurugram, Haryana, India
$5/hr · Starting at $25
KRA's include: -Authoring Narratives, Clinical Study Reports (CSRs), Protocols and Manuscripts -Medical Data Review -Punjabi Translation -Authoring and QC of Basic Results disclosed on ClinicalTrials.…
Detroit, Michigan, United States
ID Verified
$150/hr · Starting at $150
As a certified Office Ergonomics Evaluator in Office Ergonomics (COEE), I am available to perform office (or home) workstation evaluations upon request for individuals experiencing discomfort who may
Abu Dhabi, Abu Dhabi, United Arab Emirates
Preparing drugs regulatory files for submission to authorities in different countries according to the local requirements.