International Journal of Drug Regulatory Affairs

IJDRA is a broad-spectrum, open-access & peer-reviewed official Journal of Society of Pharmaceutical Technocrats (SoPhTech) circulated electronically via the world wide web. It cover the subjects - Regulatory Affairs, Intellectual Property Rights (IPR) and Pharmaceutical Development and intended to be of interest to a broad audience of pharmaceutical professionals. IJDRA now ideally placed to serve the needs of their readers and advertisers related to pharmaceutical field.  

UGC Listed Journal (Journal No. 45054)

In Index Copernicus International, Journal scored ICV of 78.1 points (2015)

Cosmos Impact Factor: 5.260

MNISW Impact Factor: 5

Scientific Journal Impact Factor Value (SJIF): 4.711

ISI Impact Factor: 0.434

Global Impact Factor (GIF): 0.454

InfoBase Index Factor: 3.73

ISOAR Impact Factor: 0.236

Our Journal is Indexed in more than 180 Databases (Highest), See Indexing

Frequency: Quarterly

ISSN:  (Print): 2321-7162 ; (Online): 2321-6794

DOI No. (From Crossref.org): http://doi.org/10.22270/ijdra.v5i2.196 (v = Volume; i = Issue; 196 Article no.)

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Phone: +91- 7096160846

Manuscripts are invited for Volume 5 Issue 3, July - Sept, 2017

Publication Charges for each manuscript is 1500 INR for Authors from India, Nepal, Bhutan, Bangladesh & Pakistan. Developing Countries: USD 50 or equivalent; Developed Countries:  USD 80 or equivalents.

Other official Journals from Society of Pharmaceutical Technocrats (SoPhTech): 

International Journal of Innovative Science and Technology (IJIST)

Journal of Drug Delivery and Therapeutics(JDDT)

Sr. no.

Courses & Events

1.

Company: ExL Events

Event: *eRegulatory Submissions Summit*

Description: Taking place July 10-11 in Philadelphia, PA, ExL Events’ eRegulatory Submissions Summit will feature in-depth discussions about best practices for the electronic submissions process and protocols for IDMP, RIMS, global and regulatory submissions. Attendees will hear obstacles submitters encounter during the preparation, filing and management of regulatory submissions and ways that industry leaders are overcoming those challenges to deliver a successful electronic submission.

Event website: http://exlevents.com/eregulatory-submissions-summit/

Emailkosmulski@exlevents.com

Contact: +1-917-242-3897 (Kelly Osmulski)

2.

Company: KNect365 Life Sciences.                                                                                        

Event: *Global Pharmaceutical Regulatory Affairs Summit *

Venue: Maritim proArte Hotel, Berlin, Germany (18-20 October 2016)                                           

Description: Streams 1 & 2: Regulatory Affairs in Emerging Markets;                                                                                       Stream 3: Global eSubmissions; Stream 4: Pharmaceutical Labelling

The Global Pharmaceutical Regulatory Affairs Summit brings together 200+ professionals across the pharmaceutical regulatory community, providing first hand case study examples of successful strategies, ample opportunity for discussion, and the opportunity to ask the experts your questions. Get practical feedback on regulatory affairs for successful product registration in the emerging markets; receive vital global updates and EU telematics guidance for optimised eSubmissions; and gain key insight and practical advice for optimised labelling information.

Event website: lifesciences.knect365.com/global-pharma-regulatory-affairs

E-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Contact: +44(0) 20 7551 9325 (Joanne Driscoll)

3.

Company: Global Leading conferences.                                                                                        

Event: *4th Annual Pharmacovigilance Forum, 29-30 Sep 2016*

Venue: Berlin, Novotel Berlin Mitte Hotel                                                                       

Description: Top pharmacovigilance experts across the world will gather to share their experience and knowledge in the field of drug safety. The scope of GLC’s 4th Annual Pharmacovigilance Forum, is to provide a platform for these practitioners in the light of providing them the solutions to some of the pressing issues they face in their daily operations..

Event website: https://glceurope.com/4th-annual-pharmacovigilance-forum-details/

E-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Contact: +36 1 848 05 31 Martin Wolf

 

Company: Sunrise Forums                                                                                        

Event: *Formulatory 2017 Asia Pacific, 27th & 28th July*

Venue: The Westin Hotel (Tentative)                                                                       

Description: The conference will be unveiling the  challenges and exploring solutions in formulations & regulatory, production of quality API in pharma industry, chemistry in action for drug synthesis, future of pharma industries in India, IT, quality and regulatory ...... & many more.
Formulatory 2017 Asia - Pacific " Formulation & Regulatory Conference is a perfect platform to showcase and discuss with the industry leaders recent advances, latest technology and alternative strategies..

Event website: 

E-mail: This email address is being protected from spambots. You need JavaScript enabled to view it. ; This email address is being protected from spambots. You need JavaScript enabled to view it.

Contact: + 91 9769327551 /+ 91 9987095030 / + 91 7400160604

 

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JOURNAL by IJDRA PUBLISHING GROUP is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Based on a work at http://www.ijdra.com/index.php/current.
Permissions beyond the scope of this license may be available at http://www.ijdra.com/images/COPYRIGHT.pdf.

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