DDREG Pharma Pvt. Ltd.
DDReg Pharma to participate in DIA Annual Meeting 2023 Boston.
DDReg Pharma is excited to announce its participation in the DIA Global Annual Meeting 2023
top of page
DDREG Pharma Pvt. Ltd.
May 1, 20232 min read
Understanding the Role of Regulatory Affairs in Product Development
Every stage of pharmaceutical product development- all the way to commercialization- relies heavily on regulatory affairs to help ensure...
18 views0 comments
DDREG Pharma Pvt. Ltd.
Apr 28, 20232 min read
What Are Purple and Orange Books in the Pharmaceutical Industry?
Introduction Manufacturers must adhere to several regulatory guidelines in the pharmaceutical industry when developing new drugs or...
20 views0 comments
DDREG Pharma Pvt. Ltd.
Apr 24, 20233 min read
Revamp Your FDA Compliance Game with Regulatory Submission Software
Introduction FDA compliance is necessary for pharmaceutical and medical device companies to bring their products to market. However, the...
6 views0 comments
DDREG Pharma Pvt. Ltd.
Apr 17, 20232 min read
What Is The Scope of Pharmaceutical Regulatory Affairs in The USA?
Pharmaceutical Regulatory Affairs (RA) in the United States encompasses a vital function that ensures pharmaceutical products comply with...
49 views0 comments
DDREG Pharma Pvt. Ltd.
Apr 5, 20232 min read
What is an ICSR? Individual Case Safety Reports
An Individual Case Study Report (ICSR) is a report that contains information about an individual patient experiencing an adverse event or...
23 views0 comments
DDREG Pharma Pvt. Ltd.
Mar 30, 20233 min read
What is regulatory intelligence and why is it important?
Regulatory intelligence forms a crucial part of regulatory operations and services that helps support and facilitate a successful...
23 views0 comments
DDREG Pharma Pvt. Ltd.
Mar 30, 20233 min read
What is eCTD? Electronic Common Technical Document.
eCTD stands for "electronic Common Technical Document." It is a standardized format for submitting regulatory information to health...
51 views0 comments
DDREG Pharma Pvt. Ltd.
Mar 6, 20233 min read
Drug Registration Process in South Korea- DDReg Pharma
South Korea is one of the largest pharmaceutical markets in Asia, making it an attractive destination for pharmaceutical companies...
157 views0 comments
DDREG Pharma Pvt. Ltd.
Feb 23, 20232 min read
What is GxP?
GxP, or Good X Practice, refers to regulations and guidelines enforced in various industries to ensure that products are safe, effective,...
44 views0 comments
DDREG Pharma Pvt. Ltd.
Feb 14, 20232 min read
Pharmacovigilance Regulations in Pharmaceuticals: An Overview
Pharmacovigilance is the science and activities related to detecting, assessing, understanding, and preventing adverse effects or other...
17 views0 comments
DDREG Pharma Pvt. Ltd.
Feb 9, 20232 min read
Choosing the Right eCTD Submissions Vendor: A Comprehensive Guide
Electronic Common Technical Document (eCTD) submissions are critical to drug development. Therefore, choosing the right vendor is...
11 views0 comments
DDREG Pharma Pvt. Ltd.
Feb 2, 20232 min read
Expert Guide to Aggregate Reporting: Types, Challenges and Solutions
What is Aggregate Reporting? Aggregate reporting is a systematic approach to monitoring and evaluating a drug's safety profile and...
15 views0 comments
DDREG Pharma Pvt. Ltd.
Jan 31, 20233 min read
What is Regulatory Information Management Software (RIMS)?
RIMS, or Regulatory Information Management System, is a software solution designed to assist with regulatory compliance for the...
71 views0 comments
bottom of page