Adequate Resources:
Experienced Stuff, Validated Processes, and Qualified Production Lines.
Commitment Partner:
Punctual Timings and Productivities with Wide Ranged Capacities.
Oral Liquid Dosage Forms:
Solutions, Syrups, Suspensions in 60 mL to 1 L Bottles.
Oral Solid Dosage Forms:
Powders in 5 to 15 gm Aluminum (ALU) Sachets and in 50 gm to 25Kg ALU or Low-Density Polyethylene (LDPE) Sachets in Cans or Plastic Jars.
Microbiological and Chemical Quality Control:
Perform All Necessary Pharmacopeial and Non-Pharmacopeial Testing.
Analytical Methodology and Validation:
Develop and Validate Any Required Method of Analysis.
Stability Studies:
Conduct Long-term, Accelerated and Stress Stability Studies
Customized Formulation:
Develop Formulations for Different Dosage Forms According to QbD Principles.
Process Development:
Develop Manufacturing Processes with Their Design Space and Control Strategies.
Technology Transfer:
Transfer the Developed Processes and Analytical Methods to Different Sites and Scales.