Pharma Services

Pharmaceutical enterprises worldwide benefit from the unique application know-how and experience of the Ortiv-Q3 Pharma Services team in solving the many issues related to dissolution and release testing from pharmaceutical dosage forms. Our staff, who specialises in in vitro dissolution testing, has a track record of determining the best technique for a wide range of goods, including implants, semi-solids, APIs, tablets, and many more. Situated in a US FDA-inspected facility, our staff's scientific experience combined with state-of-the-art instrumentation offers best-in-class services and ease of regulatory compliance for our customers. We operate in a cGMP-compliant setting with strong quality control standards.

For Experts.
By Experts.

Request a QUOTE Arrow Right

Sample Management.

Sample Management.

Reliable results require that your samples be kept under regulated conditions at all times. Strict handling procedures carried out by skilled lab personnel utilising cutting-edge equipment guarantee optimum repeatability and shield your test findings from outside influences.

Testing & Analysis.

Testing & Analysis.

In what we do, we are specialists. Our team can conduct a wide range of tests and analytical analysis since our pharmaceutical professionals are skilled in all analytical procedures and because our laboratories are furnished with equipment from various manufacturers.

Compliant Documentation.

Compliant Documentation.

Compliance is the foundation of all we do, including test execution and documentation. You can count on our paperwork to adhere to all relevant international standards, regardless of whether your service calls for thorough research to be filed with regulatory bodies or only involves basic test reports.


Experts
for Experts.

Experts
for Experts.

Our international team of professionals assists pharmaceutical firms across the globe in resolving the several obstacles related to the creation and evaluation of pharmaceutical dosage forms. Situated at a US FDA-inspected facility with cGMP compliance procedures, our staff's scientific background combined with cutting edge equipment guarantees best-in-class service.

MORE

Our Pharma Services relies on a fundamental understanding of the requirements of multiple disciplines.

R&D Services –
For your formulation.

R&D Services –
For your formulation.

With decades of experience in creating procedures for pharmaceutical items, we provide exclusive knowledge. Such competence encompasses knowledge of small and big compounds, immediate or modified release dosage forms, oral and parenteral modes of administration, and formulation as well as analytics.

MORE

Our global team of experts helps pharma companies worldwide overcome challenges in developing and testing pharmaceutical dosage forms. Our US FDA-inspected facility with cGMP compliant processes, scientific expertise, and state-of-the-art instrumentation ensures best-in-class service.

Routine Testing
Services (GMP).

Routine Testing
Services (GMP).

Are you trying to find regular GMP testing and related services in a facility that has been inspected by the US FDA? Our 100% compliance and first-rate services are made possible by our state-of-the-art lab equipment, cGMP-compliant atmosphere, and proven scientific know-how.

MORE

Our US FDA-inspected facility offers routine GMP testing and associated services in a fully cGMP-compliant environment.

Support Services –
Need help?

Support Services –
Need help?

Our unique knowledge based on decades of experience and interactions with health agencies can be of great assistance for your particular problem, whether you need to identify potential causes and solutions for your specific problem throughout the product lifecycle or need to review analytical and clinical data from a failed bioequivalence for troubleshooting in order to de-risk the next steps of development.

MORE

A comprehensive understanding of the various sectors that impact results, including API characteristics, formulation composition, manufacturing processes, and biopharmaceutical performance prediction, is essential to fully realize its potential.

Three Labs.
One Philosophy.

Three Labs.
One Philosophy.

Are you seeking for an accredited pharmaceutical facility to conduct release testing for the European Union (EU), the United States (USA) or Asia-Pacific (IN)? Do you need help creating your analytical method, or would you want to carry out in-vitro bioequivalency and characterisation investigations in order to save money on expensive human research? SOTAX has specialised Pharma Services labs with local specialists covering several fields for your unique problem across three continents.

MORE

SOTAX operates Pharma Services labs on three continents with local experts covering different disciplines. They offer certified release testing for the EU, USA, and Asia-Pacific, analytical method development assistance, and in-vitro characterization and bioequivalence studies to avoid costly human studies.

What is your
Application?

What is your
Application?

Ortiv-Q3 Pharma Services offers testing, research, and expertise to customers for every kind of dosage form. From long-acting injectables (LAI) like liposomes, microspheres, and injectable suspensions to solid oral products like tablets and capsules, as well as additional complex dosage forms like ophthalmic suspensions, coated medical devices (like stents), lotions, gels, and implants.

MORE


SOTAX Pharma Services.

SOTAX Pharma Services.

Pharmaceutical firms throughout the world benefit from the distinct application know-how and experience of the three SOTAX Pharma Services teams in overcoming the different obstacles related to dissolution and release testing of pharmaceutical dosage forms. Our teams specialise in in vitro dissolution testing and have a proven track record of finding the most appropriate method for products ranging from APIs and tablets to implants, semi-solids and many others.

Learn more about the pharmaceutical services we provide and witness firsthand the high standard of our output.

MORE

The unique application know-how and experience of the SOTAX Pharma Services team helps pharmaceutical companies worldwide in overcoming the various challenges associated with dissolution and release testing from pharmaceutical dosage forms.