Roberts Pharmaceutical Consult

After having spent 17 years in the pharmaceutical and biotechnology industries, Steve Roberts founded the company in 2002. It was his belief that companies could experience an enhanced benefit from his broad experience and knowledge in a number of inter-related disciplines, used in the development and launch of clinical and commercial supplies.

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.

A critical aspect to the cost-effective and compliant processing of any GMP material is the design, qualification and maintenance of the facility and equipment used to produce it. At Roberts Pharmaceutical Consulting we understand these realities and we place great emphasis on ensuring that client facilities and equipment meet GMP standards and are properly maintained for reliable, cost-effective performance.

Inherent in every aspect of successfully developing and launching GMP products, is compliance with industry regulations and standards. This is true throughout the entire development-commercialization cycle. It applies not only to manufacturers, but also their suppliers, vendors and contract service providers.