Welcome to BlueReg

We are an expanding regulatory affairs consultancy supporting pharmaceutical companies in their ability to develop and offer healthcare products to patients, including innovative treatment.

BlueReg provides strategy and tailored solutions to effectively overcome regulatory challenges during the entire lifecycle of medicinal products.

Our Services

Our purpose as a life science consulting firm

 

BlueReg operates since more than 10 years in the pharmaceutical industry partnering with life sciences companies in their ability to develop innovative drug products in compliance with regulations.

 

Our collaborative approach is built on our independence, our regulatory affairs hands-on experience, but also on our intrinsic understanding of the needs of pharmaceutical companies in the life sciences industry.

 

We are committed to ensure that each client enjoys optimum tailored solutions support in its regulatory affairs strategy and decision-making processes through all stages of product development, registration and launch activities.

 

We support pharmaceutical companies in their corporate strategy providing consulting services to overcome real and perceived challenges of the regulatory environment, in order to launch their innovative treatment solutions that will improve patients’ quality of life.

Fichier 2

Who do we work with?

 

BlueReg has extensive experience partnering with biotech and multinational pharmaceutical companies developing drugs for serious unmet medical needs such as Orphan Drugs in the field of rare or serious disease.

 

We also partner with pharmaceutical companies looking to optimize time to market and provide access to our extensive experience in registration strategies.

How do we work?

 

We support pharmaceutical companies with strategic consulting through all stages of product development, from clinical research, registration to the launch of innovative products on the market.

 

With our collaborative approach we aim to ensure efficient and effective interactions with health authorities protecting your projects and reputation. We also help companies to take ownership of their regulatory affairs through tailor-made solutions.

What do we offer?

 
We, as consultant for the pharmaceutical industry, offers access to cross functional teams and tailored solution to help life sciences organizations to reach their businesses objectives achieving optimum support for product development; registration and launch activities, as well as early access programs.
 
Our services will give you an additional value as we can partner with your existing internal regulatory affairs team, providing advice and access to our expertise and experts personal experience in healthcare industries.
 
For more information about Blue Reg capabilities and services offered:
 
Contact us 
ILLU HOME PAGE 3Syl

The latest resources

How to accelerate your pharmaceutical product launch in Europe?

  BlueReg is an international pharma consultancy offering strategic regulatory advice and hands-on outsourcing solutions...

Learn more

Consulting Regulatory Affairs Services for Pharmaceutical companies

  The regulatory affairs process is a critical component of the safe development, registration and...

Learn more

Pharmaceutical drug launch strategy for promotional materials in EU

As a pharmaceutical company, you want to make sure that your launch strategy in Europe...

Learn more