Aseptic Processing in the Manufacture o...
Use coupon COMPLIANCE15 to get 15% discount on this virtual seminar Sterile products may be broadly classified into two main categories based on their production mode -- those that are terminally sterilized following the filling and sealing of the container and those that are aseptically sterilized, that is, filter sterilized as a bulk product, filled, and then sealed. Aseptic Processing play a critical role with large molecules that cannot be...
Biostatistics for the Non-Statistician...
Use coupon COMPLIANCE15 to get 15% discount on this virtual seminar In today’s clinical research and biotechnology environments, decisions are driven by data. A single p-value can determine whether a promising treatment moves forward — or is left behind. For many professionals, however, statistics can feel like a foreign language. Complex software, intimidating formulas, and confusing terminology often stand in the way of confident...
Quality and GMP Compliance for Virtual...
Use coupon COMPLIANCE15 to get 15% discount on this virtual seminar Today, many companies operate on an outsourcing model. This is very common for companies who are evolving from being mainly development-focused to a point where they are entering latter stages of Phase 2 or Phase 3 clinical trials, and plan to have a product ready for market approval in the coming months. Most such companies are small, and may not have deep expertise in QA and...
Understanding REACH and RoHS Compliance...
Use coupon COMPLIANCE15 to get 15% discount on this virtual seminar This one day virtual seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others. We will review the latest on both directives and will draw out key developments and key dates (if applicable) with particular emphasis on requirements for US firms. Learning Objec...
Reduce costs for compliance with data i...
Use coupon COMPLIANCE15 to get 15% discount on this virtual seminar This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation.The instructor addres...
NEW Reclamation Process - Fed Gov't Payments
Processing ACH Reclamations from the Federal Government can be challenging! Chapter 5 of the Green Book has been updated making it mandatory for Financial Institutions to respond to all reclamations must be submitted through the Automated Reclamation Processing System (ARPS) located in Treasury’s Pay.gov web portal (except for responses by DFAS and any Treasury-approved exceptions). The Nacha Operating Rules still apply when processing t...
Quality Agreements and Their Role as Pa...
This webinar will focus on the Process for Quality Agreements and requirements that must be implemented to ensure compliance with the latest quality and regulatory requirements. Attendees will learn the reason for implementing a Quality Agreement system to assure adequate controls for Service Providers. Areas Covered in the Webinar:Regulatory Requirements for Quality AgreementsDefining the Purpose of Quality AgreementsDifferent Types of Qualit...
Guidelines for Performing a Corporate W...
Performing a corporate wide risk assessment is doable, and can provide internal audit and its organization a roadmap for the upcoming audit year. In this webinar, participants will learn how to maximize the time spent on the risk assessment process on an annual basis. Why Should You Attend:Performing a corporate wide risk assessment can seem like a daunting task for an organization. In reality, it can be done using a template and brainstorming...
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