Take control of your timeline—services offered from evaluation to validation 

Offering a wide range of services, Thermo Fisher Scientific can assist you in designing your lab, training your staff, and implementing your pharmaceutical analytics testing solution. Our experienced team has collaborated with over 4,500 labs in more than 40 countries, guiding them through the process of getting their products ready for validation. We offer comprehensive support, from initial lab setup and equipment installation to ongoing training and technical assistance.

 

We understand that releasing your product safely, rapidly, and cost-effectively is your top priority—and it’s ours, too. By collaborating with Thermo Fisher Scientific, you gain access to a wealth of knowledge and resources to help you achieve your goals. Leverage our knowledge and experience to help your lab operate efficiently and meet regulatory requirements. Let us help you bring your products to market with confidence and precision.

Design and Implementation

Let us help you streamline your path to market, leading to potential cost and time savings.

Installation and Operation Qualification (IQ/OQ)

Get started within weeks with our delivery, installation, and qualification assistance.

Computer System Validation (CSV)

Help achieve a validated state in as little as six months to outpace your competition.

Comprehensive Training

Explore training options that can help your team operate confidently and efficiently.

Regulatory Considerations

Help reduce risk and facilitate regulatory compliance with our comprehensive services.

Additional bioprocessing resources

Discover areas where you can cut costs and gain efficiency using our integrated calculator.

Explore our collection of information and insights to support your drug development journey.

Learn, evaluate, connect.                                                                                                                                 

Connect with a Bioprocessing representative or request more info.                                          

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