When you work with our company, an experienced subject-matter expert is always just a phone call away. No firm can match regulatory consultation depth of knowledge, breadth of experience and track record of success across the pharmaceutical, biologics and medical device sectors. We view each challenge as an opportunity to leverage our Industry and Agency experience in order to facilitate a better outcome for our client. With Barrolex as your success partner, you can rest assured that an experienced team of subject-matter experts with an impressive record of accomplishment in both regulatory affairs and factory setup is fully committed to helping you navigate the maze that is today new product registration process.
- We provide cost-effective quality assurance support that can save your company time and money by identifying potential problems.
- We are having an energetic team of professionals working on regulatory submissions for pharmaceutical products.
- We pride ourselves on firsthand knowledge of drug regulatory issues that span the spectrum from worldwide strategy development to post-approval activities.
- Most of our business is based on high standards, trust, and personalized attention to all projects and we want to keep it in that way to form long-term relationships.
- We maintain a network of professional associations around the world to keep current with the constant changes in regulations.
