Pharmaceutical Quality Control Testing
Accelerate your path to market with comprehensive quality control testing that meets regulatory requirements. Access GMP-compliant services that verify product safety and efficacy throughout development, helping you deliver high-quality pharmaceutical products with confidence.
What is Pharmaceutical Quality Control Testing at Element?
Pharmaceutical quality control testing verifies the safety, efficacy, and compliance of pharmaceutical products throughout their development lifecycle. At Element, we provide comprehensive analytical testing services across all phases of product development, from raw material analysis through commercial batch release, all performed in GMP-compliant, FDA-registered laboratories.
What Can Element Offer You for Pharmaceutical Quality Control Testing?
Materials and products we test
Materials and products we test
Support your entire product development cycle with comprehensive testing of raw materials, active pharmaceutical ingredients, intermediates, excipients, and finished products. Our analytical capabilities deliver complete testing coverage from initial development through commercial release, helping you maintain consistent quality throughout your manufacturing process.
- Raw materials and APIs
- Intermediates and excipients
- In-process samples
- Finished pharmaceutical products
Key tests offered
Key tests offered
Access comprehensive analytical services that verify product quality and compliance at every development stage. Our testing programs support your regulatory requirements while maintaining efficient development timelines.
Our quality control testing services include:
- Analytical method development and validation
- Compendial and monograph testing (USP, EP, BP, JP & ICH)
- Method verification
- Raw material testing
- QC testing of excipients
- In-process sample analysis
- Finished product, batch, and lot release testing
- Stability studies, including ICH stability testing and storage
- Photostability studies and photodegradation
- Forced degradation studies
- Impurity and contamination analysis
- Cleaning validation and environmental monitoring
- Extractables and leachables (E&L) studies
- Analytical support for all stages of CMC development
- Analytical trouble-shooting
- Technology transfer
Which labs offer this service
Which labs offer this service
Our team operates from Life Sciences hubs across the world, providing global access to our expert capabilities. Find out where your nearest Life Sciences hub is on our Locations Page.
Regulatory compliance support
Regulatory compliance support
Navigate complex regulatory requirements with confidence through our GMP-compliant testing services. Our FDA-registered laboratories provide comprehensive documentation and expert guidance to support your regulatory submissions.
- GMP-compliant testing
- FDA registration
- Multiple pharmacopeia testing
- Complete documentation support
- Regulatory guidance
Standards we test to and materials we test
- USP
- EP
- BP
- JP
- ICH guidelines
Raw materials
- Active Pharmaceutical Ingredients (APIs)
- Excipients
- Intermediates
In-Process materials
- Process samples
- Intermediate products
Finished products
- Final drug products
- Commercial batches
Your Challenges, Our Solutions
Quality and compliance made seamless
Complex analytics simplified
Development timelines accelerated
Technical challenges solved
Why Choose Element
Global testing network
Complete testing solutions
Expert consultation
Customized programs
Frequently asked questions
What stability testing capabilities do you offer?
Our stability testing includes ICH stability testing, storage conditions, photostability studies, and forced degradation studies to support your product development and registration requirements.
Explore our global network of labs and find your nearest location
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