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Courses

  • 1 Request Info

    Webinar on Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

    What are the strategies to be implemented before your laboratory undergoes a GMP inspection. Join the webinar to learn more. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Laboratory-Inspection-Readiness-Implementing-GMPs-for-the-Pharmaceutical-Laboratory-504036/JANUARY-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on FDA Precedent: Procedural Steps to Issue a Mandatory Recall of Herbal Drug

    Join this instructive program, where speaker will set forth the facts that how can a food mandatory recall authority be used against a drug? Register Today. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/FDA-Precedent-Procedural-Steps-to-Issue-a-Mandatory-Recall-of-Herbal-Drug-502773/JANUARY-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Good Documentation Practices and Recordkeeping Regulations (FDA & EMA)

    Discuss the importance of good documentation practices/GDP and how to create lab notebook policies that meet regulators expectations. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Good-Documentation-Practices-and-Recordkeeping-Regulations-FDA-EMA-508525/MAY-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Medical Record Standards: What Hospitals Should Know about the CMS Hospital CoPs & Proposed Changes in 2018

    Join the expert speaker Sue Dill Calloway who will cover in detail the CMS hospital cops, regulations and interpretive guidelines for medical records. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Medical-Record-Standards-What-Hospitals-Should-Know-about-the-CMS-Hospital-CoPs-Proposed-Changes-in-2018-506567/MAY-2018-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on Cal/OSHA Update for 2018: Hot Spots & Practical Compliance Strategies Every Safety Pro Should Know

    Gain insight on recent and upcoming Cal OSHA regulatory developments and trends that will impact California employers in 2018-which is right around the corner. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Cal-OSHA-Update-for-2018-Hot-Spots-Practical-Compliance-Strategies-Every-Safety-Pro-Should-Know-508509/APRIL-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On GMP Auditing of Facilities Performing Cell-Based Methods

    Laboratories that perform cell-based methods must meet stringent GMP guidelines for analytical procedures. In addition, standard operating procedures that specifically address working with cells should be in place to maintain control of a live assay system. GMP inspections should cover additional topics in cell-based laboratories to confirm procedures are sound from a regulatory perspective.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/GMP-AUDITING-CELL-BASED-METHODS-506592/AUGUST-2017-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Current Topics on Management of GMP Data Integrity

    Over 40 warning letters cited data integrity issues in 2016, and the trend has continued in 2017. This webinar gives an overview of the current regulatory climate regarding data integrity, including regulators' expectations for ensuring that the data lifecycle is integral. Highlights from the recent publications by FDA, MHRA, IPSE, and WHO will be discussed, as well as strategies for prevention, detection, and remediation of issues will be explained.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/GMP-DATA-INTEGRITY-509710/AUGUST-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On New Elemental Impurities Tests for Pharmaceutical Products according to the new ICH Q3D and USP 232/233 Guidelines: Are you ready for Janua

    The deadline for implementation of the new elemental impurities guidelines for drug products and ingredients is fast approaching. Implementation is scheduled for January 2018, by which manufacturers of pharmaceutical drug products must comply with USP <232>/<233> and ICH Q3D.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/ICH-Q3D-USP-232-233-ELEMENTAL-IMPURITIES-508597/JULY-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Measurement Uncertainty for Calibration and Testing Laboratories

    This course provides a comprehensive presentation of the principles of measurement uncertainty analysis for direct and multivariate measurements and measurement systems. Knowledge of the uncertainty of measurement of testing and calibration results is fundamentally important for laboratories, their clients and all institutions using these results for comparative purposes. Uncertainty of measurement is a very important metric of the quality of a result or a testing method.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/UNCERTAINTY-CALIBRATION-TESTING-LABORATORIES-506003/JULY-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Common Problems and Mistakes in Method Validation in Drug Development Process

    Validation of test methods is a critical requirement for the drug development process. Testing of drug substance and drug product for quality requires validated methods. In addition, testing samples for PK/PD studies requires methods that are consistent, robust, rugged, sensitive, and specific in a variety of matrices. Collecting sufficient data prior to validation that can reliably support acceptance require is a frequent issue.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/DRUG-DEVELOPMENT-PROCESS-509856/JULY-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On ISO/IEC 17025:2017 Update: The New Standard for Laboratory Competence

    This course is a comprehensive review of the changes made to ISO/IEC 17025 during its recent revision. In this course, you will be guided through the impact to your existing ISO/IEC 17025 compliant system, as well as the necessary steps to ensure compliance to the new standard.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/ISO-IEC-17025-2017-UPDATE-LABORATORY-COMPETENCE-507671/JUNE-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Proactive Internal Auditing -The Key to Establishing, Maintaining, and Improving Quality Systems

    Internal auditing is an independent, objective assurance and consulting activity designed to add value and improve an organization's operations. Conducting internal audits in the pharmaceutical and medical device industries is a key element of a quality management system. It is also a regulatory requirement and therefore a company must have a documented and systematic approach to conducting internal audits.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/PROACTIVE-INTERNAL-AUDITING-506392/JUNE-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Improving Process Stability and Capability - Tips, Traps and Guidance

    Learn the "What", "Why" and "How" of improving process capability and stability. Topics discussed include: FDA Guidance, pharma and biotech industry experience, pitfalls to avoid, sampling procedures and data quality.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/IMPROVING-PROCESS-STABILITY-CAPABILITY-508219/JUNE-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On System Suitability, Allowable Adjustments, and Data Quality in Chromatographic Systems

    This webinar provides a concise overview of the role of System Suitability testing to establish and maintain the reliability of chromatographic data quality. Rather than simply being a trivial but necessary barrier to generating chromatographic data, this webinar provides an overview explaining the essential role of a well-designed System Suitability in allowing the assurance of the continuing quality and reliability of the data generated by the chromatographic system. This webinar discusses the applicability of USP Allowable Adjustments in routine analysis, investigations and method development. A discussion of investigating System Suitability failures is included.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/DATA-QUALITY-CHROMATOGRAPHIC-SYSTEMS-508114/JUNE-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Compliance with ICH GCP R2 Addendum for Auditors

    This New ICH GCP E6 Revision 2 changes will cover those new requirements for running clinical trials, evaluate the changes and discuss how to implement these for sponsors, CROs and study sites. This session will enable you to meet the new international GCP standard to ensure the acceptance of clinical trial data by the regulatory authorities internationally including the European Union (EU), Japan, the United States, Canada and Switzerland.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/COMPLIANCE-ICH-GCP-R2-ADDENDUM-AUDITORS-505313/JUNE-2017-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On When the OSHA Inspector Visits - Will you be Ready?

    This webinar will provide you practical tips on dealing with an OSHA inspection. OSHA does not always give fair warning before they show up at your door. Roughly 36% of OSHA inspections result from employee complaints. If OSHA comes knocking today, would you be prepared? There is a positive way to handle the inspection and a negative way - handling it wrong, both before and after the inspection, can cause more problems for your company than the initial reason for the investigation.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/OSHA-INSPECTOR-VISITS-505676/MAY-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Stability Studies and Estimating Shelf Life

    This webinar discusses the steps to set-up a stability study and analyze the results to estimate the product's shelf life. The use of regression models to model the relationship between the response variable(s) and time are presented. Models useful for describing non-linear degradation over time are also presented. Additionally, methods for handling non-normal response data are also discussed. Finally, the use of accelerating variables to shorten the study time and the models required are introduced. The webinar includes several examples to illustrate the methods discussed.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/STABILITY-STUDIES-ESTIMATING-SHELF-LIFE-508052/MAY-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Statistical Approach to Monitor the Lab Operation

    Everyone in a laboratory under compliance knows about 3-sigma out-of-control issues. Can the operation be monitored to avoid these? How? This webinar will cover the basic statistics of compliance and non-compliance and how to use a statistical approach to monitor the operation to ensure that it is under control and to see when a problem is arising, but before it is outside of 3-sigma.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/STATISTICAL-APPROACH-MONITOR-LAB-OPERATION-507231/MAY-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

    Total Organic Carbon (TOC) is a useful analytical method for cleaning validation studies, including design, qualification and routine monitoring. While there may be some confusion with the industry and regulatory bodies about the use of this analytical technique, it is widely used because of certain benefits. The basis of TOC as an analytical technique will be covered, involving the various technologies currently utilized. Cautions in sampling and analyses will be discussed, including the appropriate use of blank and controls.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/TOC-ANALYSIS-CLEANING-VALIDATION-509928/MAY-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Falsifying Data in Clinical Trials: What to Report?

    Falsifying data in clinical trials is also considered data fraud. When data fraud occurs there are most likely other unreported or undetected misconduct that occurred within a clinical trial. This leads to poor, unreplicable results. When results cannot be replicated, questions arise about why a trial was conducted and what types of risks or harms were the participants exposed to.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FALSIFYING-DATA-CLINICAL-TRIALS-502132/MARCH-2017-ES-TRAININGREGISTRY