Our Services – Pharmaceuticals & Veterinary Medicine
Oral solid dose healthcare testing
Oral Solid Dose Healthcare Product Solutions for the Pharmaceutical and Veterinary Medicine Industries
CEMAS offers a comprehensive oral dose (tablet/capsule/caplet) testing service designed to designed to ensure regulatory compliance, enhance product performance, and maintain batch-to-batch consistency. We provide tailored testing solutions, for every stage of development and production of your oral dose pharmaceutical product.
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Oral Solid Dose Product Testing Services:
- Content Uniformity Testing: To verify that the active ingredient is evenly distributed across each oral solid dose product, ensuring accurate dosage and compliance – Find out more
- Disintegration Testing: To measure how quickly a oral solid dose product breaks down in a controlled environment. This test helps determine whether your formulation allows for the appropriate release of active ingredients within the required timeframe for both human and veterinary applications – Find out more
- Dissolution Testing: Assesses the rate and extent of active ingredient release from oral solid dose products using dissolution testing. This ensures that your product releases the drug as expected, therefore it offering optimal bioavailability – Find out more
- Hardness (Crushing Strength) Testing: Oral solid dose products must withstand physical stress during handling, packaging, and transportation. Our hardness testing evaluates the mechanical strength of your products, ensuring they maintain their integrity during processing and distribution – Find out more
- Friability Testing: Friability testing determines the tendency of an oral solid dose product to chip or break when subjected to mechanical forces. This test ensures that your product remains intact throughout its lifecycle, maintaining appearance and dosage integrity – Find out more
- Weight Variation Testing: Ensures that the weight of each oral solid dose product is within the specified range, providing uniform doses across the entire batch – Find out more.
- Moisture Content Testing: Excess moisture can affect the stability and shelf life of oral solid dose products. Moisture content testing therefore evaluates the amount of water in your tablets, ensuring long-term stability and preventing premature degradation – Find out more
- Assay of Active Ingredients: To accurately quantify the amount of active ingredient in each oral solid dose product, ensuring that your product contains the correct dosage – Find out more
- Stability Testing (Accelerated and Long-Term): To evaluate an oral solid dose product responds to various environmental conditions such as temperature, humidity, and light – Find out more
- Appearance Testing: A visual inspection for aspects such as colour, shape and texture, to ensure consumer acceptance and marketability – Find out more
- Veterinary-Specific Oral Solid Dose Product Testing: Veterinary formulations often require unique considerations, including dissolution rates, and bioavailability for different animals.
- Dissolution Profile Comparison: To ensure batch-to-batch consistency, ensuring therapeutic equivalence across your product lines – Find out more
Why choose CEMAS?
Science
Our scientists and study directors bring decades of experience and expertise
Compliance
GLP, GCP and GMP compliance to ensure that your regulatory needs are met
Delivery
Flexibility and responsiveness to your requirements, to provide quality data on time
Reliability
Quality and delivery are at the heart of all we do