At Roberts Pharmaceutical Consulting, we are highly experienced at developing, implementing, trouble-shooting, and optimizing GMP-compliant operations. All of our work is focused on the creation of reproducible processes, which consistently yield a high quality product at optimal cost.
We can do this because we have in-depth knowledge and experience with multiple manufacturing, packaging and warehousing technologies, which can be tailored to your unique products and business needs.
Our experience includes the set-up, qualification and validation of Manufacturing, Packaging, & Warehousing Operations for a number of GMP compliant materials. These include:
- DRUG PRODUCTS: Powders, Beads, Solids, Liquids, Semi-solids, Steriles
- ACTIVE PHARMACEUTICAL INGREDIENTS (APIs)
- BULK PHARMACEUTICAL CHEMICALS (BPCs)
- DIETARY SUPPLEMENTS & NUTRACEUTICALS
- COMPONENTS & SUPPLIES (Bottles, Labels, Syringes, etc.)
- MEDICAL DEVICES
Beyond commercial supplies of the aforementioned materials, we routinely work with the following unique materials:
- CLINICAL TRIAL MATERIALS (CTMs)
- DEA CONTROLLED SUBSTANCES
- PENICILLINS & CYTOTOXINS
- STEROIDS, POTENT, & TOXIC COMPOUNDS
- SOLVENT-BASED MATERIALS
- MATERIALS WITH A LOW MINIMUM IGNITION ENERGY RATING
Several of our customers have used our services to develop and implement significant cost savings in their operations. We have done so through:
- Improving processes and unit operation efficiency.
- Maximizing process yields and minimizing scrap rates.
- Minimizing on-hand inventories.
- Identifying more cost-effective suppliers.
- Enhancing operational practices for facilities & equipment.
Contact us at 610-361-9541 or info@pharmleader.com to review your particular operational needs.
