Showing 1–50 of 60 results
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Lifecycle Management of Analytical Methods and Procedures – according to new FDA and USP guidelines: 2-Day In-Person Seminar
February 3-4, 2020 - San Francisco, CAView Details | Register -
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar
February 6-7, 2020 - San Francisco, CAView Details | Register -
Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar
February 6-7, 2020 - San Diego, CAView Details | Register -
Designing and Sustaining New and Existing Product Stability Testing Program: 2-day In-person Seminar
February 13-14, 2020 - San Francisco, CAView Details | Register -
Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar
February 20-21, 2020 - Salt Lake City, UTView Details | Register | Download Brochure -
Detecting and Preventing Internal and External Fraud: One Day In-Person Seminar
February 21, 2020, Raleigh, NCView Details | Register -
Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR: 2-day In-person Seminar
February 26-27, 2020 - Scottsdale, AZView Details | Register -
HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer: One and half day In-Person Seminar
February 26-27, 2020 - San Francisco, CAView Details | Register -
BSA/AML/OFAC Risk Assessments – Are You Doing Them Correctly: One and Half Day In-person Seminar
February 27-28, 2020 - Dallas, TXView Details | Register -
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations: 2 days in-person Seminar
February 27-28, 2020 - San Francisco, CAView Details | Register -
A Comprehensive View of FDA Regulations for Medical Devices: 2 – Day In-Person Seminar
March 5-6, 2020 - San Diego, CAView Details | Register -
Preparing for FDA’s New Import/Export Trauma in 2020: 2-Day In-Person Seminar by Ex-FDA Official
March 19-20, 2020 - San Francisco, CAView Details | Register -
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH): 2-Day Workshop
March 23-24, 2020 - San Francisco, CAView Details | Register -
Biostatistics for the Non-Statistician: 2-Day In-Person Seminar
March 23-24, 2020 - San Francisco, CAView Details | Register -
Internal Audit, Fraud Risk Assessment and Risk Management Annual Plan: 2-Day Workshop
March 26-27, 2020 - Los Angeles, CAView Details | Register -
Data Integrity: FDA/EU Requirements and Implementation: 2-Day Workshop
March 26-27, 2020 - San Diego, CAView Details | Register -
Managing Your FDA Inspection: Before, During and After: 2-Day In-Person Seminar by Ex-FDA Official
April 2-3, 2020 - Chicago, ILView Details | Register -
REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance: 2-Day In-Person Seminar
April 2-3, 2020 - Tampa, FLView Details | Register -
Quality Control Laboratory Compliance – cGMPs and GLPs: One and a Half-day In-person Seminar
April 16-17, 2020 - Boston, MAView Details | Register -
Biocompatibility Testing for Medical Devices: One and a Half Day In-Person Seminar
May 7-8, 2020 - San Francisco, CAView Details | Register -
FDA’s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies: 2-day In-Person Seminar
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CAPA and its Strategy: Root Cause Analysis: 2-day In-person Seminar
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Building a Risk Based Internal Audit Plan: What Matters to the Organization: 2-Day In-person Seminar
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Beyond HIPAA: Developing Your Privacy and Information Security Programs in Healthcare Organizations: One and a Half Day In-person Seminar
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Smart Tax and Accounting Solutions for Small Business: 2-day In-person Seminar
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Biotech/Biosimilar Products: Current and Emerging Analytical CMC Expectations: 2-Day In-Person Seminar
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Enterprise Risk Management: 2-day In-person Seminar
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Statistical Analysis for Product Development: 2-day In-person Seminar
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Payroll Best Practices: 10 Areas You Must Handle Correctly to Ensure Compliance: One and a Half day In-Person Seminar
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Individual Tax Minimization Strategies for 2015: 2-day In-person Seminar
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TurboEIRs and their Use within Warning Letters to Illustrate the FDA and Health Canada CFRs: 2-Day In-Person Seminar
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California Laws Regulating Employment Screening and Safe Hiring: 2-Day In-Person Seminar
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Deviation Investigation Best Practices – Ensuring Correct Content and Conclusions: 2-Day In-Person Seminar
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Reducing Taxes and Managing Accounting for Efficient Business Investments: 2-day In-person Seminar
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Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices: 2-day In-person Seminar
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Global Food Supply Chain Risk and Blue Ocean Strategy Using Supply Chain Management: 2-day In-person Seminar
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Internal Control Best Practices for your Procure to Pay (P2P) Process: 2-Day In-Person Seminar
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Import Procedures and Documentation: 2-Day In-Person Seminar
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Quality Management, GMP and Regulations – Impact on Food, Seafood and Nutritional Supplements: 2-Day In-person Seminar
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Aseptic Processing Challenges: 2-Day In-Person Seminar
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Drug Master Files (DMF) – Translating FDA Guidances into Usable Documentation: One and a Half-day In-person Seminar
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Identity Theft Exposure and the Methods Utilized to Prevent and Detect the Transfer of Illegal Funds through Financial Institutions: 2-Day In-Person Seminar
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Fraud Evaluation Tools for the Internal Auditor: 2-Day In-Person Seminar
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Implementing a Basel III and COSO Compliant Operational Risk Management Program: 2-Day In-Person Seminar
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Internal Audits and Supplier Audits for Life Science Companies: 2-day In-Person Seminar
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Regulated Laboratory Inspections – Be Prepared, Be Validated and Avoid Observations: 2-Day In-Person Seminar
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