8th International Conference on cGMP, GCP & Regulatory Affairs

June 08-09, 2018 ∣ Baltimore, USA

Short Name: Regulatory Affairs 2018

Conference Theme: Meeting standards of drug regulations & achieving GxP compliance

 

About conference

Conference Series LLC is a renowned organization that organizes highly notable conferences throughout the globe. Currently we are bringing forth “8th International Conference on cGMP, GCP & Regulatory Affairs” (Regulatory Affairs 2018) scheduled to be held during June 08-09, 2018 at Baltimore, USA. The conference invites all the participants across the globe to attend and share their insights and convey recent developments in the field of Regulatory Affairs, Manufacturing of pharmaceuticals in pharmaceuticals development.

 

Regulatory Affairs 2018 is a unique platform to meet fellow key decision makers and experts all-around the Pharmaceutical, Biotech, Biomedical, Academic Institutions, Healthcare Institutes, regulatory scientists, regulatory professionals, quality analysts, formulation scientists and researchers making the congress a perfect platform to share experience, foster collaborations through the research talks & presentations to put forward many thought provoking strategies. It's a perfect stage to brainstorm, discover new ideas, search for new skills and a platform to show your capabilities and discoveries to the world.

 

Sessions/Tracks:

♦ Regulatory Affairs

♦ Regulatory Affairs in Pharmacovigilance

♦ Clinical Affairs & Regulatory Strategies

♦ Regulatory Strategies and Developments

♦ Penalties for Regulatory Non-compliance

♦ Biologics & Biosimilars

♦ Global Regulatory Intelligence

♦ Impact of Brexit on Regulatory Framework

♦ Regulatory Communications and Submissions

♦ Marketing Authorizations

♦ Regulatory Requirements for Pharmaceuticals

♦ Regulatory Challenges for Medical Devices

♦ Medical Device & Combination Products Regulations

♦ Best Industry Practices

♦ Intellectual Property Rights

♦ Current GMP Guidelines (cGMP) & GxP in Pharmaceuticals

♦ Role of c in cGMP

♦ Good Clinical Practices & Good Laboratory Practices

♦ Softwares in GMP and GCP

♦ GMP in Food Industry

 

Who should attend???

With members from around the world focused on learning about pharmaceutical manufacturing, qualitative and quantitative analysis, regulatory affairs and the most recent techniques, developments, and the newest updates in this field; Target audience expected for this conference include Pharmaceutical Manufacturing Industries, professionals from regulatory bodies, Medical Devices Manufacturing industries, Pharmaceutical Faculty, Regulatory Associations and Societies, Pharmaceutical Researchers, Pharmaceutical students, scientists, Pharmaceutical Entrepreneurs, consultancies offering regulatory affairs courses and many more.

To know more visit: https://regulatoryaffairs.pharmaceuticalconferences.com

 

Good Reasons Not to Miss Regulatory Affairs 2018

1. You can listen to world-renowned speakers.

2. The program focuses both to scientific value and impact on the industrial world.

3. You can meet companies and stakeholders in the regulatory field.

 

About Organizer:

Conference Series LLC organizes a conference series of 3000+ Global Events with over 1000+ Conferences, 1200+ Symposiums and 1200+ Workshops in USA, Europe & Asia with support from 1000 more scientific societies and publishes 700+ Open access journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.

 

Contact:

Kasper Dave
Program Manager
Direct: (702) 508-5200 Extn: 8018

Email: regulatoryaffairs@pharmaceuticalconferences.org

Website: https://regulatoryaffairs.pharmaceuticalconferences.com/