In the pharmaceutical industry, regulatory artwork services are critical to ensuring that products are safe and effective for consumers....

DDReg Pharma is excited to announce its participation in the DIA Global Annual Meeting 2023

Every stage of pharmaceutical product development- all the way to commercialization- relies heavily on regulatory affairs to help ensure...

Introduction Manufacturers must adhere to several regulatory guidelines in the pharmaceutical industry when developing new drugs or...

Introduction FDA compliance is necessary for pharmaceutical and medical device companies to bring their products to market. However, the...

Pharmaceutical Regulatory Affairs (RA) in the United States encompasses a vital function that ensures pharmaceutical products comply with...

An Individual Case Study Report (ICSR) is a report that contains information about an individual patient experiencing an adverse event or...

Regulatory intelligence forms a crucial part of regulatory operations and services that helps support and facilitate a successful...

eCTD stands for "electronic Common Technical Document." It is a standardized format for submitting regulatory information to health...

South Korea is one of the largest pharmaceutical markets in Asia, making it an attractive destination for pharmaceutical companies...

GxP, or Good X Practice, refers to regulations and guidelines enforced in various industries to ensure that products are safe, effective,...

Pharmacovigilance is the science and activities related to detecting, assessing, understanding, and preventing adverse effects or other...

Electronic Common Technical Document (eCTD) submissions are critical to drug development. Therefore, choosing the right vendor is...

What is Aggregate Reporting? Aggregate reporting is a systematic approach to monitoring and evaluating a drug's safety profile and...

RIMS, or Regulatory Information Management System, is a software solution designed to assist with regulatory compliance for the...