PCL Research&Manufacturing

PCL Research&Manufacturing is listed as a new startup research supplier in the Scientist.com network, with 2 sites in 1 country.

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Search companies, drugs, suppliers and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Sites 2

Countries 1

Type of company: New startup

API Physical Characteristics Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
Dissolution Profiling Measure release of API from formulation (tablet or capsules) under GMP guidelines.
Hot Stage Microscopy (HSM) Visualize and characterize temperature-dependent phase transitions in pharmaceutical solids, polymers, and amorphous dispersions using polarized light microscopy coupled with a controlled thermal stage.
Solid State Nuclear Magnetic Resonance Identify molecular structure or impurities and assess product integrity of solid samples.
Solubility Studies Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
Structural Chemistry Examine the relationship between protein structure and function.

Analytical Development and Validation Request services related to Analytical Development and Validation
API and Drug Product Stability Testing API and Drug Product Stability Testing.
API manufacturing process development, tech transfer and validation API manufacturing process development, tech transfer and validation
API/ Excipients Compatibility Studies Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
API/DP specific test methods API/DP specific test methods (e.g., stability indicating HPLC assay and purity)
Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services

Show all 13 in Chemistry, Manufacturing and Controls (CMC) 7 more

Compendial test methods Run Compendial test methods (e.g., KF)
Drug Formulation Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
Milling, grinding, spray-drying Milling, grinding, spray-drying
Polymorph Screening Screen for unwanted API forms resulting from the drug formulation process.
Quality by Design Quality by Design (QbD) is a proactive, scientific approach to product development that builds quality into a product from its conception, rather than relying on final end-product testing.
Salt Form Selection Use high-throughput automated arrays to combine APIs with multiple salts and ions to optimize formulation.
Thermal Analysis Characterize compounds based on calorimetry and thermodynamic data.

Show all 23 services 11 more

Production Process Consulting Use expert advice to identify sustainable improvements for manufacturing process operations.

Compound Synthesis Synthesize small molecule candidates for use in hit followup, lead optimization and medicinal chemistry.

Processing Techniques Investigation of mechanisms and kinetics of specific reactions for the improvement and stability of bioactive compounds.

Publications Plan Development & Management Strategic planning and oversight of all research dissemination activities, including outlining target journals, timelines, authors, and compliance for clinical data publications.

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