Accredited laboratories
ISO/IEC 17025 accredited partner laboratories.
Testing & Analytical Services
BEMCON coordinates specialist testing of pharmaceutical materials and finished dosage forms through laboratories suited to the assignment. Findings support quality review; batch disposition and product-release decisions remain with the client’s authorised quality personnel.

BUILT AROUND YOUR REQUIREMENT
Each engagement starts with the required outcome, operating context and evidence of success. The result is a focused Pharmaceutical Testing scope with clear responsibilities and handover points.
ISO/IEC 17025 accredited partner laboratories.
Sampling plans and chain-of-custody from site to laboratory.
Testing to ISO, ASTM, EN, GSO and SASO methods.
Certified reports with interpretation and next steps.
8 SPECIALIST CAPABILITIES
Select the capabilities that match your Pharmaceutical Testing requirement, operating context and agreed delivery stage.
Verify specified identity characteristics of active ingredients, excipients and other pharmaceutical materials. Methods and acceptance criteria are confirmed before testing.
Measure active-ingredient content in appropriate materials or dosage forms. Results are reported against the agreed specification for review by authorised quality personnel.
Arrange analysis of specified impurities using appropriate methods and reporting limits. Results identify deviations requiring formal investigation through the client’s quality system.
Coordinate dissolution testing where relevant to the dosage form. Test conditions and assessment criteria are established against the applicable product requirements.
Assess dosage-unit uniformity using an appropriate method and sampling arrangement. Findings support review against the agreed finished-product specification.
Arrange microbial testing appropriate to the pharmaceutical material or dosage form. The programme defines required tests, sample quantities and acceptance criteria.
Coordinate sterility testing where required by the dosage form and specification. Laboratory suitability, methods and sample-submission requirements are confirmed before testing.
Arrange bacterial endotoxin testing where appropriate to the product. Results are assessed against specified requirements, with deviations referred to the client’s authorised quality team.
HOW WE WORK
A defined workflow keeps the work aligned with the approved scope and makes progress, decisions and handover easier to manage.
Scope your requirementConfirm the sample or product, applicable specification and decision the testing must support.
Agree specimens, operating conditions, measurements, methods and acceptance criteria before work begins.
Manage the assignment with an appropriate specialist partner laboratory and keep the agreed scope visible.
Present measured results, observed changes, deviations, limitations and priorities for any further investigation.
WHAT YOU RECEIVE
Defined samples, methods, reporting expectations and assessment criteria before testing starts.
Testing coordinated with partner laboratories selected for the required analytical methods.
Documented results, observations, deviations and limitations for the scope actually completed.
Priorities for review, corrective action, further analysis or specialist investigation where needed.
GET IN TOUCH
Choose the type of request and share the details. The right BEMCON team will respond.