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This compliance training search contains list of all the Compliance courses scheduled as Live Webinars or available as Webinar recording links and CDs. The training catalogue features – course topics, short description, instructor's name, industry category, training level, available training option type (Live date, Rec, CD) and price.

Currently ComplianceOnline has over 700 courses across 25 industry areas. Please find/search the training/Webinars by industry category or by keyword and filter the courses by Basic, Intermediate and Advanced level. Select the trainings of your choice and add to cart, discount is available and gets reflected in cart for multiple training purchases.
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Training Name Instructor Category Training Level
OnDemand Live CD
Price
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Note – OnDemand Recording and CD of scheduled Live webinar trainings will be available after completion of the live webinars.
Engineering and Laboratory Mythology with Water System
T.C Soli Pharmaceutical  
Wednesday, September 8, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Controlling Change to meet GMP Requirements
John E Lincoln Pharmaceutical Intermediate to Advanced 
Thursday, September 9, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Key Factors to Write an Effective Standard Operating Procedure (SOP)
Kim Huynh-Ba Pharmaceutical  
Thursday, September 9, 2010
$ 249
The role of Analytical Program to Support Drug Development Process
Kim Huynh-Ba Pharmaceutical  
Tuesday, September 14, 2010
$ 249
Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
Nanda Subbarao Pharmaceutical  
Friday, September 17, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Medical Device Changes and The 510(k)
John E Lincoln Pharmaceutical Intermediate to Advanced 
Tuesday, September 21, 2010
$ 199
OnDemand Recording
$ 249
CD
$ 450
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Kimberly Kiner Pharmaceutical  
Wednesday, September 22, 2010
$ 199
OnDemand Recording
$ 249
CD
$ 450
The Hero of Manufacturing Contamination Control -- The Microbiology Lab
T.C Soli Pharmaceutical  
Wednesday, September 22, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Stability Program to support Shipping and Distribution of Drug Products
Kim Huynh-Ba Pharmaceutical  
Wednesday, September 22, 2010
$ 249
GMPs in Biopharmaceutical Development Laboratories
Nanda Subbarao Pharmaceutical  
Friday, October 1, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
How to Investigate Water System Contamination with Example Case Studies
T.C Soli Pharmaceutical  
Thursday, October 14, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Preparing for and handling FDA Laboratory GMP inspections
Nanda Subbarao Pharmaceutical  
Friday, October 15, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Importance of Method Validation Protocols and components of MVP in the Laboratory
Brian Jones Pharmaceutical  
Friday, October 15, 2010
$ 199
OnDemand Recording
$ 249
CD
$ 450
Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137
Mark Dott Pharmaceutical  
Wednesday, October 20, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Why and How - Verification of Compendial Methods - USP <1226>
Nanda Subbarao Pharmaceutical  
Tuesday, November 30, 2010
$ 249
OnDemand Recording
$ 299
CD
$ 500
Logical Water System Validation
T.C Soli Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
2010 Changes to the EU Variation Rules, Classifications and Submittal Requirements
Robert J Russell Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Software Verification and Validation Planning
John E Lincoln Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
FDA Clinical Trial Requirements, Regulations, Compliance and GCP (Good Clinical Practice)
Carol Owen Pharmaceutical  
CD
$ 500
Quality by Design - Integrating your product and process development into your submission with QbD
Peter Calcott Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 450
Nonclinical Drug Safety Evaluations in Drug Development
Paula J Lapinskas Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Drug Master Files (DMF's) - Understanding and Meeting Your Regulatory and Processing Responsibilities
James Harris(PhD) Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
Basics of testing associated with sterilization validation and routine processing
Gerry O Dell Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 450
The Odds are Against Auditing: Statistical Sampling in Audit
Steven Walfish Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Clinical Statistics for Non-Statisticians. An Introduction to Statistical Concepts and Practices
Robert S Hoop Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Conducting Successful Product Complaint Investigations
David Dills Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Fraud & Abuse in healthcare sales and marketing – Update on the Law and Tips on Compliance
Mark DuVal Pharmaceutical Intermediate 
OnDemand Recording
$ 349
CD
$ 600
GxP (GLP, GCP, GMP) Computer Validation – Change Control and Periodic Review
Michael Funk Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO)
Jamie Jamshidi Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Statistical Methods for Assay Validation
Steven Walfish Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
GxP (GLP, GCP, GMP) Computer Validation – User Requirements
Michael Funk Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
GxP (GLP, GCP, GMP) Computer Validation – Concepts and Essential Elements
Michael Funk Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 299
CD
$ 500
GMP auditor training for pharmaceutical companies
James Harris(PhD) Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 349
CD
$ 600
Understanding Disinfectant Qualification Studies – How to avoid errors
Ziva Abraham Pharmaceutical Advanced 
OnDemand Recording
$ 299
CD
$ 500
Out-of-Specification Investigations – Beyond the laboratory
John G Lanese Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 249
CD
$ 450
Auditing the QC Microbiology Laboratory for FDA Compliance
Chitra Edwin Pharmaceutical Intermediate 
OnDemand Recording
$ 349
CD
$ 600
Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
Ziva Abraham Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Appropriate and Lawful Off-Label Dissemination
Mark DuVal Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 349
CD
$ 600
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Peter Calcott Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 450
Conducting a risk assessment for objectionable microorganisms
Frank Settineri Pharmaceutical  
OnDemand Recording
$ 349
CD
$ 600
Supplier Qualification and Oversight: How to Cope with a Global Supply Chain
Paula Shadle Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
Presenting Risk Information in Drug and Medical Device Promotion: FDA's Update on Draft Guidance for Industry
David Dills Pharmaceutical Basic to Intermediate  
OnDemand Recording
$ 249
CD
$ 450
Updated EU filing and registration procedures (including the new variation rules coming in to force)
Robert J Russell Pharmaceutical  
OnDemand Recording
$ 399
CD
$ 700
Handling OOS Test Results and Failure Investigations
Dr. Ludwig Huber Pharmaceutical  
OnDemand Recording
$ 399
CD
$ 700
Japan – Regulatory Requirements and Compliance Processes for Life Science Products – Part II
Robert J Russell Pharmaceutical  
OnDemand Recording
$ 399
CD
$ 700
Important requirements when validating sterilizing grade filters
Maik Jornitz Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
Carol Owen Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 450
Managing Immunogenicity Risk in Biopharmaceuticals
Ana Menendez Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
GLP Compliance Audits: What to look out for at a New Nonclinical CRO
David Pepperl Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Statistical Sampling Plans for Audits
Steven Walfish Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Why investigators often lose money in conducting sponsored clinical trials
Stephen Schwartz Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Clinical Research Organization Audit for Good Clinical Practice
Ron Schoengold Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Principles of the Facility design for sterile manufacturing
Vadim Klyushnichenko (Ph.D.) Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
CGMPs for Investigational Drugs and Biologics
Barbara Immel Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Mastering Change Control Before It Masters You - An Essential Course for Drug Master File ’Owners’ AND Finished and Supplied Product Manufacturers
Amy E Fortenberry Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Microgranules: How can you develop and manufacture them without the need of specialized equipment?
Claudio Cerati Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Application of Process Analytical Technologies (PAT) for Eff
Keith Bader Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Dry Powder Inhalers: Why could it be the future for pulmonary delivery?
Claudio Cerati Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Cleaning Validation Swab Recovery Studies and Analysis
Keith Bader Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
ICH Q10; moving from GMPs to a Pharmaceutical Quality System
John G Lanese Pharmaceutical Advanced 
CD
$ 500
Implementing Disposable Technologies in a GMP Facility: A case study
Peter K Watler Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Water System Compliance - Successful Sanitization Approaches for Trouble-Free Water Quality
T.C Soli Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms?
Frank Settineri Pharmaceutical Intermediate to Advanced 
CD
$ 500
Out-of-Specification Investigations, Identifying the Attributable cause or Laboratory Error
John G Lanese Pharmaceutical Basic to Intermediate 
CD
$ 500
Post Market Surveillance in Today's Regulatory Environment
Judy M Andrews Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Water System Compliance - Reducing Water Microbial Excursions and Improving Investigations
T.C Soli Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
How to Write an ICH-Compliant Clinical Study Report
Robert S Hoop Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Change Management for Regulated IT Processes
Sam Mistretta Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Information Technology Change Control in cGMP regulated environments
Sam Mistretta Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Equipment and Process Change Control in Bio/Pharmaceutical Industry
Vadim Klyushnichenko (Ph.D.) Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 149
CD
$ 350
CROs (Clinical Research Organizations) – Identification, Selection, and Management for Maximum Results & Value
Robert J Russell Pharmaceutical  
OnDemand Recording
$ 349
CD
$ 600
Solutions for addressing microbial excursions in Medical device, Pharmaceutical, and Biotech industries
Jim Polarine Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
Effective Method Transfer of Complex Bioassays
Ana Menendez Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Introduction to Process Capability (Cp, CpK, Pp, Ppk)
Lawrence Mucha Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Six Sigma Methodology for Process Validation
Lawrence Mucha Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 350
Objectionable Microorganisms in an Aseptic Environment
Frank Settineri Pharmaceutical Intermediate to Advanced 
CD
$ 500
Cell Culture Media Filtration - Points to Consider
Maik Jornitz Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities
Robert J Russell Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Validation of Potency Bioassays for Biologicals
Ana Menendez Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Water System Compliance - Understanding and Controlling Endotoxin
T.C Soli Pharmaceutical Intermediate 
CD
$ 500
Failure or OOS Investigation for Sterility or Bioburden Testing
Gerry O Dell Pharmaceutical Basic 
CD
$ 500
European Filing & Registration Procedures
Robert J Russell Pharmaceutical Advanced 
OnDemand Recording
$ 299
CD
$ 500
Keys to Successful Validation Strategies for Disinfectants
Jim Polarine Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
Validation of Bioanalytical Assays for Biologicals
Ana Menendez Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Designing Regulatory - Compliant Clinical Research Data Management Systems
Dale Hunscher Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
FDA’s Current Thinking for Industry cGMPs for Phase 1 INDs
Sandra N. Whetstone Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Water System Compliance - Implementing Changes to a Validated System
T.C Soli Pharmaceutical Intermediate 
CD
$ 500
Latin America – Understanding Regulatory Compliance Requirements Across Life Science Industry Part II
Robert J Russell Pharmaceutical Advanced 
CD
$ 500
Viral Validation for Biopharmaceuticals
Kathryn Martin Remington Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Viral Safety of Biopharmaceuticals from Process Development to Licensure
Kathryn Martin Remington Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 299
Experiences of managing a quality management system for a virtual pharmaceutical company
Simon Forster Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Objectionable Microorganisms: Considering the Risk
Frank Settineri Pharmaceutical Intermediate to Advance 
CD
$ 500
Japanese PAL – JPAL change notifications and reporting between the foreign manufacturer, MAH and PMDA
Phil Smart Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Technology Transfer of a Pharmaceutical Manufacturing Process
Rodney E Thompson Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Designing Viral Clearance Studies for Biopharmaceuticals
Kathryn Martin Remington Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Latin America – Understanding Regulatory Compliance Requirements Across Life Science Industry PART I
Robert J Russell Pharmaceutical Advanced 
CD
$ 500
Ensuring the Microbiological Integrity of Pharmaceutical and Biopharmaceutical Facilities
Frank Settineri Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 199
CD
$ 350
Japanese PAL – JPAL QMS requirements in Ordinance 169 and differences to ISO 13485
Phil Smart Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Water System Compliance - What Makes Water Systems Have Microbial Quality Problems
T.C Soli Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
PROCESS ANALYTICAL TECHNOLOGY (PAT): The Impact on Pharmaceuticals Manufacturing and Validation Needs/Requirements
Gamal Amer Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Basic Requirements for Steam Sterilizer Validation per ISO 17665
Mark Dott Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Verification of Compendial Methods Understanding the New USP Chapter <1226>
Dr. Ludwig Huber Pharmaceutical Advanced 
OnDemand Recording
$ 299
CD
$ 500
Common Problems and Mistakes in Method Validation in drug development process
Dr. Wise Blackman Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 249
CD
$ 500
Pharmaceutical Manufacturing Process Validation
Rodney E Thompson Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
How to set up a small-volume radiopharmaceuticals manufacturing facility
Shankar Seetharaman Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Japanese PAL – Dealing with a JPAL Quality Interface Agreement between the foreign manufacturer and MAH (Marketing Authorization Holder)
Phil Smart Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Sterilization as a Benchmark for Cleaning Validation and Control
Anthony DeMarinis Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Validation Challenges for Bioassays
Dr. Wise Blackman Pharmaceutical Intermediate 
OnDemand Recording
$ 299
CD
$ 500
Training Requirements and Practices to Assure QSR and ISO Compliance
Jeff Kasoff Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
An Overview of Design and Development Planning
Ellen Golds Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Tort Law and Strict Liability for FDA Regulated products-What every Regulatory Affairs and Quality Professionals should know
Robert J Michalik Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 249
CD
$ 500
Parallel trade of medicinal products in the EU - Latest case law and Commission decisions
Hector Armengod Pharmaceutical Advanced 
OnDemand Recording
$ 249
CD
$ 500
Validation of Immunogenicity Assays for Biologicals
Ana Menendez Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Managed Pharmaceutical Care 101 - Understanding the marketplace and how to form strategic partnerships with Managed Care Organizations
Alan Bayham Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Drugs, Quality, and Satisfaction - Quality Improvement Initiatives by Managed Care Organizations
Alan Bayham Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Outsourcing analytical and pharmaceutical development
Michael Gamlen Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Cleaning Validation Regulations for Biopharmaceuticals: Strategies for Compliance
Paula Shadle Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Radiation Dose Setting - Method VDmax
Joyce Hansen Pharmaceutical Advanced 
OnDemand Recording
$ 249
CD
$ 500
Design Input: How to write requirements and modularize a product
Richelle Helman Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 99
CD
$ 199
The Importation of clinical trials materials into Europe : Tips to follow and pitfalls to avoid
Chris Barnett Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Method Development With the Intention of Minimizing OOS Results
Dr. Wise Blackman Pharmaceutical Advanced 
OnDemand Recording
$ 249
CD
$ 500
How Far is too Far? Statistical Outlier Detection
Steven Walfish Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Good Laboratory Practice Regulations
Dr. Ludwig Huber Pharmaceutical Advanced 
OnDemand Recording
$ 249
CD
$ 500
Basic HPLC Theory and Method Development
Jeff Phillips Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Making cGMP Documentation Practical
Paula Shadle Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Review of Changes to the New ANSI/AAMI/ISO 11137-2006 (Parts 1, 2, & 3) Sterilization of health care products - requirements for validation and routine control - Radiation Sterilization
Lisa Foster Pharmaceutical Advanced 
OnDemand Recording
$ 249
CD
$ 500
Implementing Clinical Trial Performance Metrics
Dr. Carla Hagelberg Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 149
CD
$ 350
cGMP System Strategies for Cost effective Compliance
Garry Bandel Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Improving the Quality of Pharmaceutical Product Safety Reporting through the use of Metrics
Dr. Carla Hagelberg Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 249
CD
$ 500
The Changing Face of Pharmacovigilance and Drug Safety Compliance and Inspections: Implications and Best Practices for Companies Marketing Drugs in EU
Dr. Elliot Brown Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 249
CD
$ 500
FDA’s cGMPs for the 21st Century Initiative
Betty Jones Pharmaceutical Intermediate 
OnDemand Recording
$ 249
CD
$ 500
Japanese PAL – Navigating the Japanese Pharmaceutical Affairs Law
Phil Smart Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Auditing and Compliance of Biopharmaceutical API Facilities
Frank Settineri Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 299
CD
$ 500
Update of Pharmaceutical law in the EU -Focus on Generic Opportunities & Biosimilars
Elizabethann Wright Pharmaceutical Basic 
OnDemand Recording
$ 249
CD
$ 500
Violation...Deviation: Whatever you call them, you need a process to manage them
Tina D Forrister Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Maintenance and Calibration of Equipment
Michelle Sceppa Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 450
Investigations of Microbial Data Deviations
Scott Sutton Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Virtual Manufacturing - how to manage third party contract manufacturers
Peter Calcott Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Frank Settineri Pharmaceutical Intermediate to Advanced 
OnDemand Recording
$ 199
CD
$ 350
Validation of Rapid Microbiological Methods
Scott Sutton Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach
Michelle Sceppa Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 450
Delivering Biopharmaceutical Facilities in a Risk Based World: The Role of GEP, QbD, and E2500
Jeff Odum Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations
Jim Polarine Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Cleaning & Cleaning Validation; an Overview
Gamal Amer Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 350
Auditing Strategies for Cleaning Processes and Cleaning Validation
John Hyde Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 350
Skilled and Trained for the GXP Environment: Training That Works
Dr. Wise Blackman Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 350
Corrective And Preventive Action: CAPA-A Risk Mitigating Quality System
Gamal Amer Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies
John Hyde Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Deploying Regulatory-Compliant Clinical Research Data Management Systems
Dale Hunscher Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Validating Disinfectants for Pharmaceutical and Biotech Operations
Jim Polarine Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Online Training for Laboratory Compliance- Pack of two courses
Dr. Ludwig Huber Pharmaceutical  
CD
$ 800
How to conduct a Clinical Trial in accordance with FDA regulations and how to avoid the common deficiencies observed during FDA clinical audits
Elizabeth Bergan Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 350
Deviations and Process Failures within a CAPA program
Michelle Sceppa Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 299
Regulatory requirements on pharmaceutical packaging materials from US and EU points of view
Paul Chen Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
A Practical Approach to Microbial Data Deviation Investigations
Frank Settineri Pharmaceutical Intermediate to Advanced 
CD
$ 500
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements
Carl Anderson Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Optimization of R&D project portfolio
Vladimir Shnaydman Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
How To Build Quality Into Commissioning And Validation
Jeffery Gassman Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
The New Dietary Supplements CGMPs
John E Lincoln Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Effective CAPA Management: How to Implement a Risk-based Approach to Improve Your Quality System
Ken Peterson Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Preparing Compliant eCTD Submissions
Antoinette Azevedo Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Investigator responsibility/Legal commitment in drug and device clinical research: the reality
Charles H Pierce Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How
Charles H Pierce Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Clinical Trials Process: Study Sponsor’s and Investigator’s Responsibilities
Elizabeth Bergan Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
ASTM (American Society for Testing and Materials) E2500: A New Approach to Validation
Peter K Watler Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Cleanroom Operation, Maintenance and Operators
Nazia Dar Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 350
Bringing Compliance To Design Control For Older Products
Rob Braido Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Clearing up Roles and Responsibilities in the GLPs
Anne E Maczulak Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms
Jim Polarine Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Principal Investigator responsibility in Research Involving Human Subjects: The International Conference on Harmonization (ICH) view
Charles H Pierce Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
GxP Computer Systems Validation: The Investigator’s Point of View
Dale Hunscher Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
The Coming Impact of REMS on Pharmaceutical Marketers
William Trombetta Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Understanding the Pharmaceutical Supply Chain in China Risks, Rewards, Solutions
Richard Gaeto Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Utilizing ICH Guidelines for GCP Regulatory Compliance
Carl Anderson Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Using Electronic Health Records and Claims Databases for Rapid-Response Pharmacovigilance Studies
Alan Hochberg Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Understanding CFR part 210-211 Requirements for Drug Products
Jamie Jamshidi Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 350
Statistical Pitfalls During Method Validation
Steven Walfish Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 350
Selection and Detection of Viruses in Viral Clearance Studies
Kathryn Martin Remington Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Securing your international supply chain:What heparin and DEG have to teach us
Paula Shadle Pharmaceutical  
OnDemand Recording
$ 199
CD
$ 450
Safety Risk Management for the Pharmaceutical Industry
Edwin L Bills Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Validation Requirements Based on ICH Q9
Jamie Jamshidi Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Principles of Sterile Manufacturing
James Harris(PhD) Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Pharmacovigilance aspects of licensing agreements
Dr.Sidney Kahn Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Pharmaceutical Cleaning Validation
Jeff Phillips Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Organization of Clinical Datasets in eCTD Submissions
Antoinette Azevedo Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
NEW Guidance for Industry: CGMP for Phase I Investigational Drugs
Jamie Jamshidi Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 350
Transitioning Complex Cell-Based Bioassays from the Non-Regulated Lab to the GMP Test Facility: Executing a Successful Transfer
Dr. Wise Blackman Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Understanding the Current FDA Requirements for Raw Materials and Components
Jamie Jamshidi Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
FDA Inspections-Dos & Don’ts
Ashish Talati Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Understanding Single Sampling Attributes Acceptance Sampling for Defectives. Going beyond ANSI Z1.4 and ISO 2859
John F Haury, Ph.D,CQE,CQM Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Getting the Most Out Of Data Mining for Pharmacovigilance and Risk Management
Alan Hochberg Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms
Jim Polarine Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Strategies for an Effective Root Cause Analysis and CAPA Program
Jeff Kasoff Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
The CAPA Trap or Common Problems and Pitfalls
Jeff Phillips Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Understanding Good Cell Culture Practices, GCCP, in Nonclinical In Vitro Safety Studies
Ann Wright Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Applying Lean Documents to a Project - how to create a project file, follow design controls, yet maintain a lean set of project documents
Jose Mora Pharmaceutical  
OnDemand Recording
$ 149
CD
$ 299
Orchestrating the Integration of Multiple Technical Suppliers in a Clinical Trial
Richard Barrett Pharmaceutical Basic to Intermediate 
OnDemand Recording
$ 249
CD
$ 500
FDA’s Expectations for cGMPs for Analyst/Process Chemists
Sandra N. Whetstone Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Implementing Process Controls for Optimum Performance of Cell-Based Assays
Dr. Wise Blackman Pharmaceutical  
OnDemand Recording
$ 299
CD
$ 500
Implementing Quality Management Systems in Small Companies
William G Mclain Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Biopharmaceutical Viral Safety from Process Design through Validation
Kathryn Martin Remington Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Project Manage Your Validation Project -- Introduction to Initiating and Planning a Validation Project - Part 1
Lawrence Mucha Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Supplier Capability Audits - how to tell if a supplier ’gets it.’
Jose Mora Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Using Kanban/JIT Systems to Run a Startup Plant
Jose Mora Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Network Infrastructure Qualification for CGMP regulated environments
Sam Mistretta Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Cleaning Validation - Chemical & Microbiological Aspects
Nazia Dar Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Through the eyes of an auditor... how your plant looks to an auditor and how you can make the best first impression
Jose Mora Pharmaceutical  
OnDemand Recording
$ 249
CD
$ 500
Microsoft Word and Excel in FDA Regulated Industries: Pack of Four Training Courses
Pharmaceutical  
OnDemand Recording
$ 799