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  • 1 Request Info

    Webinar On Regulatory Intelligence and Exports in Food Industry

    This training will provide an understanding of what regulatory intelligence is and how to benefit from it. Attendees will learn how to perform a rigorous GAP analysis and establish an export strategy based on regulatory intelligence.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/REGULATORY-INTELLIGENCE-EXPORT-FOOD-INDUSTRY-503929/AUGUST-2017-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2

    This webinar will cover the new law on confidentiality of substance use disorder patient records under 42 CFR Part 2. This law was previously known as the confidentiality of drug abuse and alcohol abuse records. The new law was effective in 2017. Anyone or any facility that is subject to these requirements needs to attend this webinar.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/NEW-FEDERAL-LAW-42-CFR-PART-2-503438/AUGUST-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On Executing and Managing Effectively: Developing an Organizational Leadership Program

    Take the lead on helping leaders to grow, develop and flourish!. In providing your organization with a Leadership program that works, we want to utilize an approach and methodology which emphasizes developing and fostering the leadership potential in each participant and in supporting each participant's efforts to lead effectively in your organization..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/EXECUTING-MANAGING-EFFECTIVELY-503914/AUGUST-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On Implementing a Metrics Program - Uncovering and Overcoming the Challenges

    Recently the FDA released their draft guidance for industry entitled "Request for Quality Metrics". Much discussion of quality metrics has ensued regarding this guidance and its elements. This presentation provides an integrated view of the aspects of Quality Metrics including the required supporting quality culture..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/METRICS-PROGRAM-503090/AUGUST-2017-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On Quality by Design (QbD) for Analytical Methods

    There are always certain steps in a method where control is critical either because this step contributes a lot to the overall uncertainty or its uncertainty is more likely to change from common causes. These critical points can be assessed and a monitoring program instituted. This data is then collected and plotted on a control chart. Using Nelson's rules of statistical use of control charts, the individual uncertainties are monitored. This allows for early observation and intervention before a non-compliance occurs..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/QUALITY-DESIGN-ANALYTICAL-METHOD-502373/AUGUST-2017-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On HUD's Physical Inspection Process, New UPCS Rules According to REAC

    Introduces participants to HUD's Uniform Physical Condition Standards (UPCS) physical inspection protocol and procedures. Review of the new UPCS rule. This topic covers the process and procedures interesting in conduction pre-inspections to final inspections. A discussion of the REAC scoring process will be discussed in order to achieve high REAC scores and maintain your property in compliance with the new rule. How to address deficiencies in a timely manner to maintain high REAC scores.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event linkhttps://www.onlinecompliancepanel.com/webinar/HUDs-PHYSICAL-INSPECTION-PROCESS-507805/AUGUST-2017-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Leading Indicators & Trends to Predict Health Injuries and Environmental Incidents

    Leading indicators have been used for years to predict the future. Weather professionals to predict the weather use barometric pressure. Polls are used to inform politicians if they should change their strategy and elevated body temperature or blood pressure are leading indicators concerning an individual's health.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/LEADING-INDICATORS-PREDICT-HEALTH-INJURIES-503618/AUGUST-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Reducing Human Error in GMP Environments: Assure Compliance with Regulators Expectations

    This training program will offer attendees an understanding of human errors in GMP related environments, factors and causes, and control measures to be put in place to reduce the same. In this webinar we look at the common causes of Human Error in GMP manufacturing. We outline an approach to reduce these errors with an objective to offer you an insight into the common causes of Human Error and to provide you with a defined approach to investigating risk influencing factors and root cause, reducing Human Error and sustaining error reduction within your own company.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/REDUCING-HUMAN-ERR0R-GMP-ENVIRONMENTS-503587/AUGUST-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Understanding Proper Aseptic Technique and Cleanroom Behavior

    This training program will discuss how, in sterile compounding, aseptic technique is contributing to the prevention of microbiological contamination. It provides sterility, safety, and efficacy to the sterile product, especially various injections for patients. In this course, cleaning, gowning and proper methods of contamination control will be reviewed along with why cleanrooms are designed the way they are.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/ASEPTIC-TECHNIQUE-CLEANROOM-BEHAVIOR-508276/JULY-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On OSHA's Fall Protection Safety Best Practices: Understanding the Changing Requirements for General Industry and Construction

    This online training course follows OSHA requirements for fall protection training for the construction worker who might be exposed to fall hazards. This program enables the employee to recognize the hazards of falling, and trains them in the procedures to be followed to minimize these hazards. With falls from heights being the leading cause of occupational fatalities, it is not only imperative that employers train their employees; it is also mandated by law, CFR 1926.503.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/OSHAs-FALL-PROTECTION-SAFETY-506072/JULY-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On An Introduction to Risks associated with Extractables, Leachables & Elemental Impurities in cGMP Manufacturing: A Project Managers Perspect

    This webinar will present a unique perspective on risks associated with extractables, leachables & elemental impurities (ELEI) in cGMP manufacturing of pharmaceutical, biologic and medical device products. The webinar will start with a definitional review of the topic and then present the current FDA perspective on impurities of these types in product. After that introduction, the instructor will present quality and compliance considerations related to ELEI.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/EXTRACTABLES-LEACHABLES-cGMP-MANUFACTURING-507103/JULY-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    FDA Process Validation for Applied Statistics 2017

    In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, "...the collection and evaluation of data, from the process design stage through commercial production..." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle: Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities. Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing. Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control. The first stage of process validation is process design. The Process Validation guidance document states: "A successful validation program depends on information and
  • 13 Request Info

    Webinar On Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

    Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.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/PHARMACEUTICAL-COMPRESSED-AIR-502789/MAY-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Crossing the Line Online: Preventing Sexual Harassment and Sex Discrimination in the Age of Social Media

    Given the ease of receiving and viewing sexually explicit materials on cell phones, computers and social media, employers as well as employees should be concerned about claims of a hostile work environment and preventing all forms of sexual harassment in the workplace. This workshop will focus on the issue of sexual harassment, sex discrimination and how to prevent it in the workplace. It will provide an overview of sexual harassment, sex discrimination, its definition and the laws that prohibit it.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/SEXUAL-HARASSMENT-DISCRIMINATION-502025/APRIL-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Thriving with the Revised ISO 14001 Standard; Key Changes and Transition Strategies

    The ISO 14001 standard has been updated. If you presently have the ISO 14001 standard in place at your facility this webinar is a must! The webinar will address the changes to the standard.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/THRIVING-REVISED-ISO-14001-502667/APRIL-2017-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Harmonized System Classification: General Rules

    The Harmonized Tariff Schedule is an international customs classification system. It was developed by the World Customs Organization, as a tool to facilitate the world trade by creating a nomenclature that assures uniformity in its application, and at the same time address domestic issues. Not only it is used to establish tariffs and duties, but also to implement measures to protect the public health, the environment, the wild and the world safety.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/HARMONIZED-SYSTEM-RULES-508887/APRIL-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Harmonized System Classification Basics, General Rules and Sections Content: Webinar Series

    All companies involved in international trade must understand the importance of determining the correct Harmonized Tariff Schedule provision for imported and exported products. The HTS is also used to determine whether goods are subject to "other agency requirements," quotas, or free trade agreements. U.S. Customs expects companies to use reasonable care and correctly classify its imported products at the time of entry.Price:$600.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HARMONIZED-SYSTEM-CLASSIFICATIOIN-SERIES-509908/MARCH-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Harmonized System Classification: Basics

    The Harmonized Tariff Schedule is an international customs classification system. It was developed by the World Customs Organization as a tool to facilitate the world trade by creating a nomenclature that assures uniformity in its application, and at the same time address domestic issues. Not only it is used to establish tariffs and duties, but also to implement measures to protect the public health, the environment, the wild and the world safety. It has been in force since 1988. It is used for 90% of the trading world.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/HARMONIZED-SYSTEM-CLASSIFICATION-509007/MARCH-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Environmental Monitoring Investigations

    Attendees will get an overview of environmental monitoring investigations and tools to complete an investigation. Environmental monitoring is the method by which clean rooms are known to maintain a certain level of cleanliness. The methods by which clean rooms are monitored are through viable and non-viable testing. Through this testing, a room may demonstrate that it is out of control. This seminar will provide aspects to investigate in order to determine a root cause and appropriate actions to complete the report.
  • 20 Request Info

    Webinar On WHMIS 2015 - Canada's Adoption of Globally Harmonized System of Classification and Labeling of Chemicals (GHS) for Workplace Chemicals

    Canada's first major GHS deadline is just months away. Don't wait to get started on your compliance tasks! Canada officially adopted GHS on February 11, 2015 and implemented a series of phased-in compliance deadlines - the first of which is scheduled to go into effect on June 1, 2017. This session will provide a high level overview of Canada's adoption plans.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/WHMIS-2015-GHS-WORKPLACE-504341/MARCH-2017-ES-TRAININGREGISTRY