Chinchwad, Maharashtra, India
$10/hr · Starting at $25
CTD and ACTD dossiers for regulated, semi regulated markets. Having hands on experience in Pharmaceutical industry for 10 years.
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…
Surat, Gujarat, India
ID Verified
$12/hr · Starting at $48
What you deliver with this Service ** Buy with confidence ** We believe our experience with WordPress and how to use it to suite people’s unique business needs makes us a viable choice to help you g…
Cairo, Al Qahirah, Egypt
$20/hr · Starting at $25
- Preparation of registration dossiers (including CTD, ACTD and non-ctd dossiers) for pharmaceutical drug products, dietary supplements and medical devices according to country's regulations - prepara…
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…
Tamilnadu, Tamil Nadu, India
i'm already working office in CTDS TAMILNADU . experience : 1 year but ( 2013- 2016 ) 3 years i'm working marketing Executive Manager I'm interested in online works Only..
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.
Donetsk, Donets'ka Oblast', Ukraine
Medical and pharmaceutical translation (English - Russian) Translation of individual and general pharmacopoeial monographs (EP, USP, JP) Translation of validation documentation (analytical procedures,…
Bangalore, Karnataka, India
Hands on experience in Safety Data Collection, Safety Data entry, Safety Case Review, MedDRA coding,WHO Drug Coding and various reports generation e.g. PSUR, DSUR, CIOMS, MedWatch e.t.c. Expert in pre…
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.
Kolkata, West Bengal, India
I am a postgraduate (M.Pharma), having 10 years of experience in quality assurance and regulatory affairs field of Pharma and Medical Devices. Currently I am working as a quality and Regulatory Affai…
Ben Aknoun, Alger, Algeria
$25/hr · Starting at $25
I am a regulatory affairs pharmacist with more than 8 years experience in regulatory affairs. Having a good knowledge of the local pharma environment, I can support and represent companies in Algeria
Hyderabad, Telangana, India
$15/hr · Starting at $25
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…
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…
Coimbatore, Tamil Nadu, India
Have over 5 years of experience in SAS applications used in clinical trials and research on WINDOWS environment. Had been responsible for generating & validating TLFs for safety and efficacy analysis
Reggio Calabria, Calabria, Italy
$50/hr · Starting at $100
I have a Msc in electronic engineer. I am a Certified LabVIEW Developer (CLD) and a Certified TestStand Developer (CTD). I have 10 years of work experience in the SW developer for Automation Test Equi…
Amman, Amman, Jordan
Quality Management System (QMS), ISO 9001, Good Manufacturing Practices (GMP) & Good Laboratory Practices (GLP). Wide knowledge in laboratory instruments (operation/calibration) such as HPLC, UV Spect…
$70/hr · Starting at $300
Regulatory Affairs/Intelligence (Pharma/Consumer Health/MD)-(MEA/LEVANT/APAC/CIS/Others). Regulatory End to End consultation service. I am working in the field of Pharmaceutical Industries; I am a pha…
Manjeri, Kerala, India
I am experinced in formatting documents for publishing online . I also do html tagging if html files are reqiured for the project. I have also worked as editor in few magazines n english. I can also t…
$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