Testing & Analytical Services

Pharmaceutical Testing

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.

8 specialist capabilitiesSpecialist partner laboratoriesDefined success criteria
Pharmaceutical Testing
Pharmaceutical TestingTesting coordinated around your sample, specification and decision

BUILT AROUND YOUR REQUIREMENT

Pharmaceutical Testing with a clear purpose

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.

Accredited laboratories

ISO/IEC 17025 accredited partner laboratories.

Sampling

Sampling plans and chain-of-custody from site to laboratory.

Standards-based methods

Testing to ISO, ASTM, EN, GSO and SASO methods.

Reports you can use

Certified reports with interpretation and next steps.

8 SPECIALIST CAPABILITIES

What the service can cover

Select the capabilities that match your Pharmaceutical Testing requirement, operating context and agreed delivery stage.

01

Raw-Material & Ingredient Identity Testing

Verify specified identity characteristics of active ingredients, excipients and other pharmaceutical materials. Methods and acceptance criteria are confirmed before testing.

02

Active-Ingredient Content Testing

Measure active-ingredient content in appropriate materials or dosage forms. Results are reported against the agreed specification for review by authorised quality personnel.

03

Impurity Testing

Arrange analysis of specified impurities using appropriate methods and reporting limits. Results identify deviations requiring formal investigation through the client’s quality system.

04

Dissolution Testing

Coordinate dissolution testing where relevant to the dosage form. Test conditions and assessment criteria are established against the applicable product requirements.

05

Dosage-Unit Uniformity Testing

Assess dosage-unit uniformity using an appropriate method and sampling arrangement. Findings support review against the agreed finished-product specification.

06

Microbial Quality Testing

Arrange microbial testing appropriate to the pharmaceutical material or dosage form. The programme defines required tests, sample quantities and acceptance criteria.

07

Sterility Testing

Coordinate sterility testing where required by the dosage form and specification. Laboratory suitability, methods and sample-submission requirements are confirmed before testing.

08

Bacterial Endotoxin 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

From test question to usable findings

A defined workflow keeps the work aligned with the approved scope and makes progress, decisions and handover easier to manage.

Scope your requirement
  1. 01

    Define the requirement

    Confirm the sample or product, applicable specification and decision the testing must support.

  2. 02

    Build the test programme

    Agree specimens, operating conditions, measurements, methods and acceptance criteria before work begins.

  3. 03

    Coordinate testing

    Manage the assignment with an appropriate specialist partner laboratory and keep the agreed scope visible.

  4. 04

    Report and decide

    Present measured results, observed changes, deviations, limitations and priorities for any further investigation.

WHAT YOU RECEIVE

Evidence designed for the next decision

Agreed test programme

Defined samples, methods, reporting expectations and assessment criteria before testing starts.

Coordinated specialist testing

Testing coordinated with partner laboratories selected for the required analytical methods.

Clear technical findings

Documented results, observations, deviations and limitations for the scope actually completed.

Practical next steps

Priorities for review, corrective action, further analysis or specialist investigation where needed.

GET IN TOUCH

How can we help?

Choose the type of request and share the details. The right BEMCON team will respond.