Finished Pharmaceutical Products Quality Control (QC) Testing

Project Description

MULTIPLE PRODUCTS
MULTIPLE TESTING
ISO 17025 Africa Pharmaceutical Laboratory needed for quality control testing of various finished pharmaceutical products. Please respond with the following.

1 Schedule of Requirement (ToR)
2 RFQ Pricing Forms

Return completed offer forms with relevant technical and regulatory requirements, past experience and quality conformance related documents.
Required Accreditation and Certification for QC/Testing Laboratory
The Contracted QC laboratory must meet the following criteria in full:
1. Must be an ISO17025:2017 Certified for the required QC testing scope
2. Have the technical capability to adopt the in-house specifications for testing as provided by the manufacturer for non-compendia products.
3. Should be in a position to perform the method transfer process to validate the in-house method provided by the manufacturer.
4. Should be adequately equipped with appropriate equipment and should have the technical capabilities including well-qualified and trained staff to undertake the quality control on products required for testing.
5. Should be capable of communicating with the manufacturer (where required/permitted by UNOPS) in case samples are found to be out-of-specifications, to take decision to declare the products as non-compliant and advice on actions to be taken.

Required Document
Contracted QC Laboratory is required to provide the following documents with the quotation submitted.
- Valid ISO17025:2017 certificate with Testing/analysis scope
- Latest laboratory quality management audit report.

Project Information

Number:24-00733

Industry:Pharmaceuticals

This request is closed and is no longer accepting quotes. Register or Log In to receive alerts when similar requests open in the future.

Other pharmaceuticals laboratory services.

Other Pharmaceuticals testing, analysis, scientific research and development, inspection, certification, engineering, failure investigation, and product development needs include :

Drug Discovery Testing

Drug Development Testing

Non-Clinical Study Testing

Preclinical Study Testing

Clinical Trials Testing

Pharmacokinetics (PK) Testing

Pharmacodynamics (PD) Testing

ADME Testing

Sterility Testing

Pyrogens Testing

Endotoxins Testing

Raw Material Testing

Finished Product Quality Control Release Testing

Real-Time Stability Testing

Accelerated Stability Testing

Method Development Testing

Method Validation Testing

Drug Release/Dissolution Testing

Extractable Testing

Leachable Testing

Elemental Impurities Testing

Packaging Testing

Child-Resistant Packaging Testing

Container Closure Integrity Testing (CCIT) Testing

High Throughput Screening Testing

Reverse Pharmacology Testing

Excipients Testing

Active Pharmaceutical Ingredient API Testing

Toxicology Testing

Toxicity Testing

Microbiology Testing

Strength Testing

Quality Testing

Purity Testing

Consistency Testing

Acid Insolubles Testing

Acid Solubles Testing

Alkali Solubles Testing

Alkalinity Testing

Appearance Testing

Boiling Point Testing

Congealing Temperature Testing

Flash Point Testing

Melting Point Testing

Freezing Point Testing

Hardness Testing

Heat of Combustion Testing

Preservatives Testing

Loss on Drying (under Vacuum) Testing

Loss on Ignition Testing

Melting Point Testing

Mineral Analysis Testing

Non-aqueous Titration Testing

Normality Testing

Organic Acids Testing

Organic Extractives Testing

Oxidizing Substances Testing

Peroxide Value Testing

Pour Point Testing

Reactivity Testing

Reactivity to Water Testing

Reducing Substances Testing

Refractive Index Testing

Residue on Evaporation Testing

Residue on Ignition Testing

Saponification Value Testing

Sieve Analysis Testing

Silver Reducing Substances Testing

Silicon Testing

Sulfur Testing

Sodium Testing

Specific Gravity Testing

Specific Rotation Testing

Sugars Testing

Sulfur Compounds Testing

Surfactants Testing

Talc Testing

Titration Curve Testing

Total Halides Testing

Total Reducing Compounds Testing

Unburned Carbon Testing

Uncarbonized Constituents Testing

Unsaponifiable Matter Testing

UV Absorption Testing

Volatile Matter Testing

Volatile Suspended Solids Testing

Weight Variation Testing

Cytotoxicity Testing

Elution Testing

Agar Diffusion Testing

Bioburden Testing

Antimicrobial Effectiveness Testing

Particulates Testing

Total Combined Mold & Yeast (TYMC) Testing

Total Aerobic Microbial Count (TAMC) Testing

Testing

Learn more about pharmaceuticals testing and research

Finished Pharmaceutical Products Quality Control (QC) Testing

Project Description

Project Information

Test Request: 25-00933

Test Request: 25-00922

Test Request: 25-00908