The scope of the FDA document includes drugs, biologics, and positron emission tomography drugs. The agency also states the requirements are consistent with the requirements in ICH Q7, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients, thus expanding the scope of the document to APIs and drug substances. The FDA states it is the “role of management with executive responsibility to create a quality culture where employees understand that data integrity is an organizational core value. …”
Do you have control over your supply chain? Qualification of suppliers is critical to ensure only authentic products are distributed. To ensure confidence:
- the authorized supplier must have a manufacturing or wholesale dealer license
- the authorized supplier must comply with current good distribution practices (GDP); and
- you should perform periodic due diligence checks.
For additional guidance, check out this article from the Medicines and Healthcare Products Regulatory Agency (MHRA).
Did you know that the primary reason for device recalls is due to poor design control? This guidance document (“Applying Human Factors and Usability Engineering to Medical Devices” published Feb. 3 2016) is critical for both device and combination product manufacturers. It can help you establish the path for ensuring that the design of the medical device or the drug delivery system has been developed with human factors in mind to minimize potential use errors and resulting harm. Understanding how the user interface design affects interactions people have with technology and the environment where device is used can ensure the products form, fit and function addresses patient needs. This guidance includes a template of the outline and content expected of the human factor report that should be issued for each device going to market, considerations for determining sample sizes for human factors validation testing, and guidance on analyzing results of human factors validation testing.
Learn more and download the guidance document here.
How does your company handle GXP data? CGMP violations involving data integrity have been increasing over the last few years. Data integrity is an important component to ensure safety, efficacy, and quality of drugs.
This guidance document is critical for all pharmaceutical, medical device and biotechnology companies to help establish robust data handling policies and procedures. It clarifies data integrity definitions, discusses when to retain original documents, describes how to handle electronic data, when it is permissible to exclude CGMP data from decision making and much more.
Learn more and download the guidance document here.
FDA and NIH have updated the clinical trial protocol template for Phase 2 and Phase 3 IND (investigational new drug / investigational device exemption) studies.
Public comments can be submitted by April 17, 2016 via a form found on the NIH Office of Clinical Research and Bioethics Policy website under the Clinical Trial Protocol Template Documents section.
Download the protocol template shell here.
Download the instructions here.
Submit public comments on these new templates here.
MWA Consulting, Inc. is pleased to announce that Lisa Helmonds will join the MWA team as Vice President on April 1st, 2016.
“With over 30 years of industry training within the areas of Manufacturing and Quality Assurance in the pharmaceutical and medical device industries, Lisa brings significant experience and leadership to the MWA team,” says Bill Daniels, CEO. “In her new role as Vice President, Lisa will focus on developing, maintaining and growing the relationships with MWA’s clients, increasing the number of highly-qualified MWA associates, implementing training programs, and ensuring that MWA continues to offer the highest quality GXP consulting services in the industry.”
Lisa’s prior professional history includes over 13 years as an independent consultant/associate with Marion Weinreb & Associates, Inc. which became MWA Consulting in January 2016. Lisa has extensive GXP knowledge, understands the complexities of large companies and the challenges of start-ups. She holds a BS in Zoology from the University of Rhode Island and an MBA from Santa Clara University.
“I am honored to be working with Lisa in this next phase of MWA’s development,” says Marion Weinreb, President of the new corporation, and an active member of the consulting team. “Lisa brings a wealth of knowledge to MWA and embraces the values that management and the members of the MWA team demonstrate in their high touch interactions with clients, and in the consulting services that we provide.”
ABOUT MWA CONSULTING, INC: Formerly Marion Weinreb & Associates, Inc., MWA is a dynamic consulting and staffing organization with expertise in GXP (GCP, GLP and GMP) compliance. We ensure that pharmaceutical, biotechnology, and medical device companies efficiently meet and exceed their compliance goals from development through commercialization. Website: www.gxpsrus.com. Phone: 866.497.7787.
This is one of the most practical guides published to assist companies in setting up quality agreements with their suppliers. It contains practical information, attempts to identify best practices, embraces and encourages sample language and provides common sense solutions to typical issues that come up during the quality agreement process.
Rx-360 is a not for profit consortium led by volunteers from the Pharmaceutical and Biotech industry including both manufacturers and suppliers. The purpose is to enhance the security of the pharmaceutical supply chain and to assure the quality and authenticity of the products moving through the supply chain. The organization’s mission is to protect patient safety by sharing information and developing processes related to the integrity of the healthcare supply chain and the quality of materials within the supply chain.
Download the entire guide here.
IT expert advocating for stronger pharma IT security.
This article highlights the threat that hackers and cyber-criminals pose to drug and device manufacturing systems. MWA assesses the security of your IT systems during audits, particularly those that consider Part 11 compliance. If you feel that your organization is protected, read this article and share it with your IT personnel. You may want to reconsider your conclusions.
Hackers trying to steal drug formulae for counterfeiters can wreak havoc says an IT expert advocating stronger security for networked pharmaceutical manufacturing facilities.
This guidance document describes the decision-making steps that we recommend you follow to determine whether a PMA supplement should be submitted when you intend to change the manufacturing site (including a change to the processing, packaging, or sterilization site) of your legally marketed PMA-approved device. This guidance also discusses general factors FDA intends to consider to determine whether a preapproval inspection is necessary before approval of the PMA supplement.
There is a great table that outlines the type of manufacturing site changes that FDA believes affect the device’s safety or effectiveness as well as the type of submission that should be submitted to FDA. Manufacturers are responsible for validating changes, as necessary, in accordance with the QS regulations, whether or not a PMA supplement is submitted.
Download the entire guidance here.
APIC recently released a great guide for both API and drug manufacturers on dealing with foreign particles. The guideline differentiates between the different types of particles that can be present in a batch.
Technically unavoidable particles: particles which do not harm the health or safety of the final consumer. They should not affect the efficacy and quality of the related Drug Product due to the (chemical) harmlessness of the material and / or their mechanical attributes and low amount. Technically unavoidable particles are intrinsic to the manufacturing process, the production equipment and processing aids.
Atypical particles are particles that should not be present in final API and their presence should always trigger an investigation. These particles consist of foreign matter which is not intended/designed to be in direct contact with the product/manufacturing process. These atypical particles commonly originate from materials which accidentally or unintentionally came into contact with the product or a process stream.
The guide offers practical ways to minimize the presence of particles in APIs, proposals for limits on particle size, prevention measures, and much more.
Download the guidelines here.