We are leaders in the Life Sciences Industry, offering cGMP Compliance services throughout the Product Lifecycle from R&D to Commercialization in the following sectors:
Since our inception in 1993, we have focused on developing a technical, administrative, and human resources infrastructure with a single purpose: to provide integrated quality and compliance services to highly-regulated manufacturers around the globe.
Our services are under the latest FDA, EMA, ANVISA, and other international agencies' regulations and guidelines. We provide the following services to help your business excel:
• Regulatory Compliance
• Quality Management Systems
• Commissioning and Qualification
• Validation Services
• Technology Transfer
• Project Management
• Quality Risk Management
• Regulatory Affairs
• Workforce Enhancement and Talent Management
We work with clients around the Globe, offering expert knowledge and services to drive their business operations to success. Take a look at some of our work.
We have experience supporting all types of companies and under different regulatory environments from stem cells, HCT/P to large molecules or medical devices.
Integrity, commitment, and trustworthiness is what defines our company. Over the last three decades, we have become a leading employer in the Life Science Service Industry with hundreds of qualified and experiened professionals.More About US
Quality is the essence of our
Highly prepared leadership and reliable management team guarantees success
Strong regulations knowledge
and real-world expertise makes us
an invaluable partner
Our global presence ensures diversity
and cost savings
We have an extensive pool of highly knowledgeable and experienced consultants around the world
The quality of our services translates into long-term customer relationships
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