Blog | DDReg Pharma

The Importance of Quality Control in Regulatory Artwork Services- DDReg Pharma

DDREG Pharma Pvt. Ltd.

May 15, 20233 min read

The Importance of Quality Control in Regulatory Artwork Services- DDReg Pharma

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

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DDReg Pharma to participate in DIA Annual Meeting 2023 Boston.

DDREG Pharma Pvt. Ltd.

May 12, 20231 min read

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

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Understanding the Role of Regulatory Affairs in Product Development

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...

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What Are Purple and Orange Books in the Pharmaceutical Industry?

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...

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Revamp Your FDA Compliance Game with Regulatory Submission Software

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...

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What Is The Scope of Pharmaceutical Regulatory Affairs in The USA?

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...

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What is an ICSR? Individual Case Safety Reports

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...

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What is regulatory intelligence and why is it important?

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...

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What is eCTD? Electronic Common Technical Document.

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...

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Drug Registration Process in South Korea- DDReg Pharma

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...

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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,...

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Pharmacovigilance Regulations in Pharmaceuticals: An Overview

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...

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Choosing the Right eCTD Submissions Vendor: A Comprehensive Guide

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...

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Expert Guide to Aggregate Reporting: Types, Challenges and Solutions

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...

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What is Regulatory Information Management Software (RIMS)?

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...

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