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Consulting - Pharmaceuticals
Aveta has expertise regarding all equipment, utility systems and operations that relate to pharmaceuticals, GLP laboratories & manufacturing. Also, Aveta’s team has world thought leaders in Process Analytical Technology development & implementation. Our holistic approach to equipment and system includes the design, automation, qualification, validation, operation, cleaning & contamination issues, preventive maintenance and continuous compliance. Following is a representative list of areas that Aveta has hands-on experience with:
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Active Pharmaceutical Ingredients (APIs) |
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Solid Dosage: Tablets/Hard Gelatin Capsules/Soft Gelatin Capsules |
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Liquid: Syrups/Suspensions/Emulsions |
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Dry Powder For Oral Suspension |
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Semi-Solid: Creams/Ointments |
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Packaging: Primary & Secondary |
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Labeling |
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Laboratory / Analytical: R&D, In-process and QC |
Other services include:
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Characterization & Process Improvement
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Enable drug manufacturers through QbD & DFSS to develop approvable novel ways bring new ideas to the US & EU marketplaces |
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Export Opportunity
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Enable Indian companies with heightened compliance to sell to US, Canada & EU |
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Nutraceuticals:
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Ayurvedic, Homeopathic and Food Supplement dosage forms for International markets will need to meet with US GMPs, if for export to US |
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Operations
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Design assist for GXP Lab, Pilot Plant & Large Scale Bulk & Finished Dosage Manufacturing |
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Equipment selection & qualification; GMP Facility Design |
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GMP Operations Integration & GMP Supply Chain |
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All services to support market segment |
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