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Our Pharma Insights Blog

Drug Review & Approval Process in Canada

Healthcare is a public welfare endeavor and all the governments across the countries strive for…

Key Challenges and Solutions in Cryogenic Product Management

Cryogenics products contain cryogenic liquids that turn into gases under ambient temperatures. The word cryo-…

ICH Guidelines for Pharmaceuticals: Complete Overview of Multidisciplinary Standards

Drug development is primarily driven by three factors: quality, efficacy, and safety. The essential quality,…

Comprehensive Overview of ICH Safety Guidelines

To identify potential safety concerns such as unpleasant adverse effects of the medicines, ICH provides…

ICH Efficacy Guidelines for Drug Development & Clinical Trials

The mainstay of drug development is based on 3 parameters such as quality, efficacy and…

Drug approval process in China

The People’s Republic of China is a huge pharmaceutical market and big pharma companies have…

ICH Quality Guidelines: What Every Pharmaceutical Professional Needs to Know

A global initiative called the International Council for Harmonization of Technical Requirements for Pharmaceuticals for…

What are Generic Medicines and Why are They Affordable?

Generic drugs are copies of the original branded drugs that are made available in the…

What is Third-Party Manufacturing in Pharma and Its Benefits?

The manufacturing of pharmaceutical products by a third party is referred to as third-party pharmaceutical…

USA Drug Approval Process: Synthetic and Biological Medicines for Human Use

The centre for drug evaluation and research (CDER) is responsible for ensuring availability of safe…

The Role of Expanded Access Programmes in Drug Development

The development of drugs is a long process, and it takes 12-15 years to complete…

How to Optimize Clinical Trial Supply Chain Process for Faster Drug Development

Conducting clinical trials is a multifaceted activity involving several stakeholders and participants. Once the trial…

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