Information for Media Partners
International Journal of Drug Regulatory Affairs (IJDRA) is a broad-based journal giving leading international coverage of all aspects of Pharmaceutical Sciences. It publishes high quality original research & reviews. By advertising in IJDRA, you can reach the targeted audiences worldwide. Your product information disseminates internationally with comparatively low cost budget.
Regulatory Affairs professionals /Scholars, Patent agents, IPR / F&D / R&D professionals, Pharmacologists; toxicologists; Pharmaceutical researchers; Pharmacists; Clinicians, Analysts, Medical and Health Sciences etc.
While advertisements are crucial to this journal to be able to keep all content free for everyone, ethical considerations are in place to ensure the integrity of the journal and its content:
- "Pop-up" and "banner" ads appear on a random, rotating basis. The advertiser has no control or input over the pages where their ads appear.
- The Editorial Board has full and final approval over the content of all advertisements.
- Advertisers will never be shown any manuscripts or other content prior to publication.
This Journal carries an advertisement, which generates income, but journal not be dominated by advertisements, and advertising must not be allowed to influence editorial decisions. Journal follows advertising policies as per International Committee of Medical Journal Editors (ICMJE).
Advertising and Special Services Contact Information:
Company: Bluetech Media
Event: cGMP Compliances, Inspection & Investigation
(Remote & On-Site Audits)
Date and venue: 4th & 5th March 2021
This webinar provides a basic understanding and fundamental principles of Current Good Manufacturing Practices (cGMP) and will fulfill the requirement of personnel involved in cGMP must have documented training of current Good Manufacturing Practices.
This session will focus on the Current approaches to Inspection, Warning letters, Investigations, Compliances, Human Error, Invalid OS.
Personnel involved in cGMP must have documented training of current Good Manufacturing Practices (cGMP) training. This webinar will focus on the FDC Act and 21CFR federal regulations as applied to cGMP and provide an overview of the US FDA regulations for compliance.
Delegates will get an opportunity to learn from Ms. Rajni Jha, an expert trainer on QBD, GMP, and Regulatory Affairs and Mohamed Anvar Deen, CSV and IT GxP Compliance Lead at Sun Pharma.
We shall also have a few panel discussions where Pharma experts will shed their viewpoints on the subject matter.
Contact: +91 99209 08212
Company: Compliance Trainings
Event: The Annual Validation Summit-2021
Date: 25-27 February,2021 ; Venue: Online
Description: The Annual Validation Summit - 2021, conceptualized and curated by Compliance Trainings, is a benchmark event for validation, quality and IT professionals across the life sciences, providing critical information on new regulations, technology advances and industry best practices.
Event website: https://www.validationsummit.
Contact:+8867363146 (Neil P)
Company: Eminence Business Media
Event: Advanced Pharma Tech: IT & CSA Webinar
The current pandemic situation is here to revolution adaption of technology at an unprecedented rate. There has never been a better time to step up and take action in understanding and adapting the technology.
Eminence Business Media is virtually hosting the Pharma Web Summit focussing on adaptability of IT and CSV.
Event Website: https://www.eminencemedia.in/reach-out-to-us.php
Contact: Suryansh Rana +91 9653284123
Company: Professionals Regulatory Affairs Consultancy
Event: GCC Regulatory Affairs Pharma Summit 2021l Hybrid
Venue: March 22nd & 23rd .2021, HABTOOR GRAND RESORT, DUBAI, UAE & VIRTUAL
GCC Regulatory Affairs Pharma Summit is an annual event that provides platform for pharmaceutical regulatory experts and industry professionals in the GCC region to share insights and discuss about the latest updates in the pharmaceutical regulations.
This Summit is one of the first and strategic meeting place in the GCC region for local and international pharmaceutical and medical industry professionals to meet and discuss on topics related to all aspects of regulatory affairs, legal and compliance.
Event website: https://www.pramagcc.
Contact: +971 54 306 8878; Madre, Event Manager
Company: Pulsus Group
Event: International Conference on Clinical Research and Case Reports
Venue: Paris, France
Description: Pulsus Group cordially welcomes all participants around the world to attend "International Conference on Clinical Research and Case Reports" which will be held on June 29-30, 2020 in Paris, France. The theme of the conference is "Innovations and Approaches in Clinical Trials and Clinical Research". The experts can deliver the idea by Poster sessions, Exhibition, keynotes, speaker forum and Young research forum. The purpose of the Clinical Research conference is to develop interest, the transaction of ideas, stimulate research, planning for diagnosis, prohibition, remedy and recovery using clinical trials and research. This conference serves as the best platform to share your ideas and researches to the outer world. Conference attendees can also explore Paris, which has many attractive places to visit. Global centre for Fashion, Art, Gastronomy and Culture.
Event Website: https://clinicaltrials-research.pulsusconference.com
Contact: Janet Stewart( Program Manager)