CIS will offer Government Programs (GP) webinars over the summer months including lessons learned from Medicaid Managed Care Organizations (MMCO), 340B and Bona Fide Service Fees (BFSF).
Tom Evegan, formerly of Acorda Therapeutics, joins CIS as Senior Director of Commercial Contracting Services. Mr. Evegan will provide oversight of CIS' strategic Contracting Services.
APSH silicone hose is braid reinforced to handle working pressures involving fluid transfer in pharma, biotech, food and other clean process applications. Unlike silicone tubing without reinforcement, APSH with stands the pressures used when transferring large batches of liquids. APSH is sterilizable, offers documented lot traceability and quality control, and meets many industry standards.
CIS announced Pennsylvania Bio will host its breakfast symposium, "Preparing for the Sunshine Act - How to Weather the Storm of Federal and State Regulations," featuring industry experts from CIS and Cangene BioPharma.
The Triangle Business Journal announced today that Compliance Implementation Services (CIS), a leading life sciences consulting firm, is a winner in its inaugural class of the 2013 Life Sciences Awards, which recognize both individuals and organizations that are breaking ground in the life sciences field.
CIS was chosen by Covis to develop and implement a corporate compliance program and manage the ongoing compliance and requirements of Government Program (GP) participation.
Vascular BioSciences (VBS) announces it will be presenting at a National Heart Lung and Blood Institute (NHLBI) conference on June 11, 2013, from 10:30 to 5pm at the Janssen Research & Development Labs, 3210 Merryfield Row, San Diego CA 92130.
SUSdocs.org is a new website devoted to educating and informing viewers about single use/disposable systems used in pharmaceutical and bioprocess applications. The site was developed through the cooperative efforts of several pharma-related associations and suppliers. All documents are impartial, explanatory and intended to help and support the single use systems industry.
"The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on June 4. Robert J. Russell, President of RJR Consulting, Inc. will be the Speaker at this 90-minute webinar.
GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, "Statistical Process Control for Process Development and Validation" on May 23 and 24, 2013 (Thursday & Friday). Steven Kuwahara, Founder and Principal, GXP Biotechnology LLC, will be the speaker at this two-day session.
CIS will provide thought leadership at several industry-leading conferences and host four webinars to advance techniques that ensure "sunshine readiness" and identify potential operational challenges in preparation for CMS' federal transparency and disclosure collection that begins on August 1, 2013.
GlobalCompliancePanel to hold two-day, in-person seminar in Mumbai on the topic, "Software Validation for the New FDA Inspections" on July 1 and 2, 2013 (Monday and Tuesday). David Nettleton, an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation, will be the speaker at this two-day session.
Compliance Implementation Services (CIS), a leading life sciences consulting firm, announced that on Friday, May 3, CMS published its list of Teaching Hospitals in conjunction with OPEN PAYMENTS, the CMS program under which applicable manufacturers and group purchasing organizations (GPOs) will begin tracking and reporting payments and other transfers of value to physicians and teaching hospitals.
Compliance Implementation Services (CIS), a leading life sciences consulting firm, today announced that Judy Fox, Director, Transparency Compliance and Adam Toronto, Associate Director, Commercial Compliance, will speak at the 4th Annual West Coast Forum on Sunshine and Aggregate Spend, taking place in San Diego on April 23-25.
The new site design is user-friendly and provides a graphically-enhanced stroll through product showcases, nutrition news, health and wellness education, video features and Paragon Laboratories corporate highlights.
The symposium "Sunshine - How to Weather the Storm of Federal and State Regulations," held March 26 in Long Beach, featured a panel of industry experts from CIS and Advanced Orthopaedic Solutions (AOS) who discussed the key federal and state compliance and reporting requirements.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "New EU Pharmacovigilance Directive and Regulations" on April 9. This 90-minute webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data" on April 11. This webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Attribute Data" on April 11. This webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.
This course is about the Hazard Analysis and Critical Control Point (HACCP). It will introduce the role of the HACCP. It will start with a chronology of the HACCP program in the US food industry, in which it will cover important historical events and program milestones.
It is an irony of sorts that although companies that are regulated by the Code of Federal Regulations such as Title 21 and Title 493 are required by law to have Standard Operating Procedures (SOPs); there is no guidance on how to write, organize and maintain these critical guidance documents.
GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, "Software Validation for the New FDA Inspections" on April 18 and 19, 2013( Thursday & Friday). David Nettleton, an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation, will be the speaker at this two-day session.
GlobalCompliancePanel to hold two-day, in-person seminar in San Francisco, CA on the topic, "Effective Complaint Handling, Medical Device Reporting and Recalls" on April 25 and 26, 2013 (Thursday & Friday). David R. Dills, a senior Regulatory & Compliance Consultant, will be the speaker at this two-day session.
Upcoming symposium is designed specifically for medical device companies interested in learning critical strategies to better manage federal and state compliance and reporting requirements.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on April 9, 2013.Kim Huynh-Ba, Executive Director of Pharmalytik will be the Speaker at this session, whose topic will be"Key Factors to develop an effective CAPA system".
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