Medvacon Supports Compounding Pharmacies to Provide Safe and Efficacious Products

December 4, 2020 – (SPARTA, NJ) – MEDVACON Life Sciences—a Quality, Compliance and Validation consulting company—is working with compounding pharmacies to help identify gaps in quality systems to ensure that they meet current FDA requirements to supply safe and effective products. Additionally, as part of supporting the rapid start-up of a new facility, MEDVACON will be supporting the ongoing day-to-day quality operations, helping to facilitate the
rapid growth of the compounding pharmacy in a fully compliant manner. According to the U. S. Food & Drug Administration, drug compounding is often regarded as the process of combining, mixing, or altering ingredients to create a medication tailored to the needs of an individual patient. A drug may be compounded for a patient who cannot be treated with an FDA-approved medication, such as a patient who has an allergy to a certain dye and needs a medication to be made without it, or an elderly patient or a child who cannot swallow a tablet or capsule and needs a medicine in a liquid dosage form.

“MEDVACON is proud to be able to support these clients with our deep background in quality and regulatory compliance in all aspects of pharmaceuticals and FDA compliance, whether it is via a third-party quality audit or helping our clients to develop internal quality systems,” said Joe Toscano, one of the founding members of the life sciences company. “MEDVACON is helping clients meet stringent FDA regulations,” he continued, “by providing the initial core policies and procedures to support the ongoing licensing process and startup of commercial activities at new facilities.”

According to Toscano, MEDVACON is providing the initial suite of operational and policy Standard Operating Procedures (SOPs) required for GMP (Good Manufacturing Practices) compliance in the FDA-regulated 503A/B pharmacy space. “Our expertise and experience will allow our clients to begin operations as rapidly as possible in a fully compliant manner,” he added. MEDVACON is a full-service Quality and Compliance consulting firm offering a suite of quality services such as: Quality Systems Implementation and Remediation; Computer System Validation; Process and Cleaning Validation; Equipment, Facility and Utility Qualification; Mock FDA Inspections and Audits; Project Management; and cGMP Training. These services help clients to ensure FDA Compliance and reduce compliance cost in the Life Sciences’ industry. The company provides experienced project administration, trouble-shooting, and/or training services, on-site, with local resources and senior management involvement to optimize flow and collaboration. Headquartered in Sparta, NJ, MEDVACON Life Sciences also has offices in San Diego California. More information can be found at http://www.Medvacon.com.