At Ace Laboratories, we provide comprehensive analytical testing services supported by robust methodologies, advanced instrumentation, and experienced scientific professionals. Our approach is built on precision, reliability, and data integrity, ensuring that every analysis delivers accurate and meaningful results.
Through carefully controlled processes and scientifically sound methodologies, we support pharmaceutical companies in maintaining product quality, meeting regulatory requirements, and making informed decisions throughout the product lifecycle.
Analytical Testing at Ace Laboratories
We carry out analytical and microbiological testing for pharmaceutical manufacturers — finished products, raw materials, and the samples that arise across a product’s life. The work is done by experienced analysts on qualified instruments, against methods that are either compendial or properly verified in our own laboratory.
What clients are really buying from a contract laboratory is confidence in the result and a record that holds up under inspection. That is what we are set up to provide: accurate data, generated under control, documented so that it can be traced and defended
How We Run a Test
Good data starts before any instrument is switched on. Every sample is handled the same way, so the result is consistent whoever does the work.
When a sample arrives, we confirm what is being tested, against which specification, and by what method, before testing begins. We test using the relevant pharmacopoeial method or an approved, verified laboratory procedure — not an improvised one. Analysts run the work on qualified instruments under controlled conditions. The data is then reviewed independently against the specification before any result is released, and reported clearly enough that the reader can see what was tested, how, and against what limits.
Where a result falls outside specification, it is investigated and reported — not quietly set aside. That matters more than any statement about quality we could make on this page.
Methods and Standards
We test against recognised compendial methods (Ph. Eur., BP, USP) and approved internal procedures. Where a method is not compendial, or is transferred to us from a client, it is verified in our laboratory before it is used for release testing, so we know it performs reliably on our instruments, in our hands.
Instruments are qualified and kept under planned maintenance and calibration. Procedures are documented and followed. None of this is unusual for a regulated laboratory — but it is the difference between a result you can rely on and one you cannot, so we treat it as the core of the work rather than the background to it.
What We Test
We support pharmaceutical quality control across the areas a manufacturer needs covered:
Finished product testing against registered specifications. Raw material and API testing to confirm identity and quality before use. Stability testing under defined storage conditions to support shelf-life. Impurity and related-substance analysis to detect and quantify degradation products. And microbiological testing to assess product quality and safety.
Quality and Data Integrity
We support pharmaceutical quality control across the areas a manufacturer needs covered:
Finished product testing against registered specifications. Raw material and API testing to confirm identity and quality before use. Stability testing under defined storage conditions to support shelf-life. Impurity and related-substance analysis to detect and quantify degradation products. And microbiological testing to assess product quality and safety.
Discuss a Testing Requirement ?
If you have a testing requirement or want to talk through an analytical problem, our team is happy to help. Get in touch to discuss what you need and how we can support it
