Regis Technologies invites members of the pharmaceutical and biotech industries to a technical talk on metrics for drug development in Morton Grove on November 12, 2015. Guest speaker Jason J. Orloff, will present "Metrics: The Balance of Performance & Compliance."

Morton Grove, IL (PRWEB) October 31, 2015

On November 12th, Regis Technologies will host Jason J. Orloff at their GMP facility in Morton Grove, IL. Orloff will deliver a technical seminar on "Metrics: The Balance of Performance & Compliance." The talk is open to the public. Arrive at 8:00am for coffee and networking; the seminar will begin at 8:30am and will last one hour.

"Metrics: The Balance of Performance & Compliance" will assess quality initiatives in the pharmaceutical industry and will answer the questions, "Where does process capability belong? As a compliance reportable? Or as a self-audit of performance done by manufacturing for senior management to prioritize continuous improvement?"

Orloff will address how to achieve a maximally efficient pharmaceutical manufacturing sector by formalizing systems of performance and ensuring that the balance of compliance and performance is maintained.

More information, including the abstract and how to register, are available on the Metrics: The Balance of Performance & Compliance home page.

Jason J. Orloff, Ch.E. & M.S. Applied Statistics is a Principal Statistical Consultant at PharmStat. He is an international consultant specializing in applied statistics and experimental design for pharmaceutical and biopharmaceutical development, quality assurance, quality control, validation, and production under the cGXP's. Orloff brings over fifteen years of experience in manufacturing, quality, and regulatory affairs in the pharmaceutical industry. Areas of expertise include PAT, OOS, SQC, SPC, assay validation and setting specification criteria.

Regis Technologies hosts technical seminars at its Morton Grove, IL location and around the country throughout the year. This winter, Regis will also host a webinar on the IND process with a panel of experts from the drug development industry; register for "Success Factors in Your Investigational New Drug (IND) Filing" here.

Sign up today to receive email invitations to these events and watch past seminars by visiting Regis' website.

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