Total Number of Events: 1,118

 

Date: Jun 1, 2018 - Dec 31, 2019

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This training program will describe when a full investigation should be triggered and the frequency for re-testing and re-sampling. Attendees will also learn how to implement corrective and preventive action plans (CAPA).Why Should You Attend:This 90-minute accredited course is designed to provide sound training on how to recognize and investigate atypical or out of specification results, using approaches which have been recommended by regulatory...
 

Date: Jun 1, 2018 - Dec 31, 2019

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In this revised ICH GCP guideline on budgeting and contracts for clinical trial webinar will discuss the impact of changes in ICH GCP E6 R2 on investigator, site, sponsors CROs roles and responsibilities and the impact of clinical trial conducts and organizational practices along with evaluate solutions/applicability/modifications of organizational SOPs, processes, procedures and staff training; and discuss opportunities for implementing the revi...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This FDA communication best practices webinar will discuss the best practices for communication with FDA staff, general timing of communications, how to deal with deficiencies and key resources for premarket applications and post market communications.Why Should You Attend:The US Food and Drug Administration offers a range of mechanisms to communicate with premarket and premarket staff. The timing of communication and best practices to ensure bot...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This virtual seminar on Family Care and Medical Leave in California will examine the requirements for family care and medical leave, employers covered by the CFRA/FMLA, a covered employer’s duty to post notice of CFRA requirements and obligations, employees eligible for CFRA/FMLA leave, and more. The program will also explore the interplay between California’s Pregnancy Disability Leave law, CFRA/FMLA, compensation while on leave, continuatio...
 

Date: Jun 1, 2018 - Dec 31, 2019

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Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood how the writing of a procedure can have a positive or negative impact on training. In this course you will learn the vital connection between the documentation and training spheres, and how to maximize this connection to improve the quality of both SOPs and tr...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This training program will elaborate factors affecting the target weight decision and help determine the tolerable risks of under-filling and the costs of over-filling. Attendees will gain an understanding of process stability and process capability concepts and methods for process optimization.Why Should You Attend:In order to maximize profitability while complying with government regulations regarding net package contents, food manufacturers an...
 

Date: Jun 1, 2018 - Dec 31, 2019

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Discharge planning has become more than just the movement of the patient out of the hospital. It is a “process” that starts at the point of admission and follows the patient beyond discharge. The Centers for Medicare and Medicaid Services (CMS) have recently added more “teeth” to the process as it is outlined in the Conditions of Participation for Discharge Planning. Discharge planning is no longer a destination but a process that starts ...
 

Date: Jun 1, 2018 - Dec 31, 2019

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Understand the definition of New York State paid family leave and how it will impact your organization. The webinar will also discuss the process for filing, pending changes, and its association with the FMLA.Why Should You Attend:This webinar will cover:The definition of NYS paid leaveHow it will impact your organizationThe process for filingPending changes
 

Date: Jun 1, 2018 - Dec 31, 2019

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This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system.Why You Should Attend:Negative customer feedback about a medical device's performance or safety is a strong indicator of whether a firm's manufacturing process is in control. This feedback is therefore subject to many requirements in both ...
 

Date: Jun 1, 2018 - Dec 31, 2019

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In this Dietary supplements batch control webinar learn what and how to create master manufacturing records, what batch production records to create and what to do with completed batch records as per FDA 21 CFR Part 111 requirements. Learn inventory management techniques that make the creation and management of Master and Batch production records easier.Why Should You Attend:In the manufacture of dietary supplements, the FDA, under 21 CFR, Part 1...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This training program will examine how to manage the AML/KYC compliance risk, which is a critical element in a robust BSA/AML compliance program. It will also explore customer identification and on-boarding and CDD/EDD/on-going risk based monitoring.Why Should You Attend:There was a time when a wire transfer may come in with the "By Order" party listed as "My Good Customer." No longer.That statement sums up AML/KYC Risk. Essentially there is no s...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This webinar will teach attendees best practices for building a sustainable vendor qualification program for FDA regulated industries. It will discuss common pitfalls to avoid when qualifying vendors.Why Should You Attend:If you are looking for the answer to the following questions, you will certainly benefit from attending this webinar on building a vendor qualification program:Have you wasted hours, days, and weeks on qualifying vendors that yo...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This webinar will discuss the CMS requirements for standing orders and protocols in four separate sections. It will describe that all protocols must be approved by the Medical Staff even if the protocols are department specific.Why Should You Attend:CMS created a tag number to house the major section regarding standing order requirements in the medical record chapter under Tag 457. There are a total of four separate sections in the hospital CoP m...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This CBP audit preparation training program will help attendees move toward a systematic approach for both general compliance and when notified about a CBP audit. It will help identify the likelihood of being subject to CBP audits, and help spot potential vulnerabilities and test your compliance(potential vulnerability, self review, general audit issues).Why Should You Attend:The focus of the webinar rests on the recent attention given to trade i...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This webinar will explain legislative roles and responsibilities of workplace parties and how HR plays a pertinent role in it. Instructor will discuss OSHA regulations and safety compliance practices and how to create safety culture at workplace. He will share practical tips and best practices for HR managers taking the responsibility of safety regulatory compliance.Why Should You Attend:The roles of the HR professional and the safety management ...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This BSA compliance training on Suspicious Activity Reporting (SAR) will provide details on how to prepare a SAR (Suspicious Activity Reporting) narrative that meets examiner scrutiny and provides necessary detail for law enforcement.Why Should You Attend:According to the FFIEC Exam Manual: "Suspicious Activity Reporting forms the cornerstone of the BSA reporting system." "It is critical to U.S’s ability to utilize financial information to comb...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This project and alliance management webinar will present tools valuable for planning a project, identifying required outsourced activities, selecting a CDMO, monitoring/controlling an outsourced project, and communicating project performance to leadership.Why Should You Attend:In this age of nimble and efficient development organizations focused on pharmaceutical and generic product development, planning and managing outsourced activities is a b...
 

Date: Jun 1, 2018 - Dec 31, 2019

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The webinar will provide methods for assessing and understanding Process Capability. Participants should be able to immediately apply the methods presented.Why Should You Attend:This webinar discusses methods for estimating process capability for both normal and non-normal data. Pre-requisites for estimating process capability (e.g. establishing process stability) are discussed first. Distributions are briefly described and methods for estimating...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This HR data , metrics, HR scorecard course will teach how to make practical use of metrics and analytics by working through problem solving, data determination and use of data from start to finish for four of the most important functions of HR: Hiring, Performance Management, Compensation and Turnover.Why Should You Attend:HR data is comprised of both metrics and analytics. In the business of HR, both metric and analytics have their place and gi...
 

Date: Jun 1, 2018 - Dec 31, 2019

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This webinar will discuss the challenges and opportunities involved in developing and implementing an operational risk appetite statement, which is supported by operational risk limits, and the determination of actual exposure against those limits.Why Should You Attend:Regulators, credit rating agencies, board members, shareholders and other stakeholders expect that financial services companies clearly articulate and quantify their appetite for e...
 

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