Auditing of Computer System Validation to Ensure Data Integrity
Recognize the requirements for data integrity, validation activities, and documentation. Recognize an approach to inspecting computerized systems ...
Management Responsibility for Quality: What FDA Expects
Identify managements specific responsibilities in developing and maintaining a Quality System.
Data Integrity: The Role of Quality Assurance for Data Integrity
Recognize the definition and importance of a process approach to quality, and recognize activities that help maintain quality of data. Identify ...
Bloodborne Pathogens -- General Industry
Identify the risks of working around bloodborne pathogens, the controls in place to eliminate or reduce those risks, and the equipment that can help ...
Bloodborne Pathogens -- Healthcare Workers
Recognize the definition of bloodborne pathogens and identify some of the diseases they can cause. Recognize controls and procedures that can lower ...
Fire Safety for Healthcare Workers
Recognize the sources of heat, oxygen, and fuel that can start a fire. Recognize regulatory considerations for healthcare facilities regarding fire ...
Postmarket Reporting of Adverse Drug Experiences
Identify the process for reporting postmarketing adverse drug experiences to FDA.
Documenting the Drug Development Process ICH Q8(R2)
Recognize the guidance from FDA covering the documentation of pharmaceutical drug development. Identify how the guidance can be used to consistently ...
Hot Work Permits
Identify the process of hot work area evaluation. Recognize the contents of a hot work permit. Recognize the responsibilities of management, workers, ...
Q9: Quality Risk Management
Identify the methodology and tools used in a risk management process. Recognize the operational areas where risk tools can be used to increase ...
The Clinical Development Process: Investigational Product, Plan, and Data Management
Identify the steps leading to the final FDA review and approval for marketing of a new product.
FDA Establishment Inspection (EI)
Identify the statutory authority for establishment inspections. Recognize the procedures to prepare for, conduct, and conclude inspections.
Combustible and Flammable Liquids
Identify guidelines and precautions for handling, transporting, and storing combustible and flammable hazards found in your workplace. Recognize ...
Computer Workstation Safety
Identify common RSIs, their symptoms, their causes, and exercises and other safety measures that can help you prevent them.
Privacy and Data Protection
Recognize what personal information must be protected according to the law and our company policies, as well as your personal responsibility in ...
Quality Systems Approach
Identify FDAs guidance on modern quality systems and recognize how this can foster GMP compliance, innovation, and continuous improvement in the ...
QSIT 1 -- Beginning the Inspection
Recognize the origin and scope of QSIT. Recognize the basic concepts associated with how to sample records for review during an inspection conducted ...
QSIT 2 -- The Management Controls Subsystem
Identify the seven Inspectional Objectives associated with the Management Controls subsystem and recognize some of the ways to accomplish those ...
QSIT 3 -- The Design Controls Subsystem
Identify the fifteen Inspectional Objectives associated with the Design Controls subsystem. Identify some of the ways to accomplish those objectives.
QSIT 4 -- The Corrective and Preventive Actions Subsystem
Identify the ten inspectional objectives associated with the CAPA subsystem and recognize the ways to accomplish those inspectional objectives.
QSIT 5 -- The Production and Process Controls Subsystem
Recognize the six inspectional objectives of the Production and Process Controls subsystem and techniques for accomplishing those objectives.
Systems Based Drug Inspections
Recognize the guidance provided by FDA for investigators inspecting drug firms for GMP compliance. Recognize the guidance provided in CP 7356.002 ...
ICH Q7A: Introduction and Quality Management
Recognize the purpose of the Q7 Guideline and how it fits in with current regulatory expectations and practices in the United States especially in ...
Part 11: Electronic Records and Signatures -- Changes in Enforcement Policy
Recognize FDA expectations for compliance with all applicable predicate rules. Identify how the Agency plans to interpret and enforce Part 11 with ...
Part 11: Electronic Records and Signatures -- Application
Recognize how to apply Part 11 regulations to your companyÂs systems and records in accordance with FDAÂs expectations. Identify what records are ...
Part 11: Electronic Records; Electronic Signatures
Identify the regulatory requirements for electronic records and electronic signatures. Recognize FDA expectations for compliance.
Computerized Systems Inspections in the Medical Device Industry
Recognize where computerized systems are used in the medical device manufacturing process. Recognize FDAs approach to inspecting computerized ...
Physical and Network Security
Recognize security risks to our companyÂs physical and virtual assets. Identify your responsibilities for protecting all of these resources. ...
ICH Q7: Resources and Materials Management
Identify the general requirements for qualification of API manufacturing personnel. Identify the requirements for buildings and facilities as well ...
Change Control
Identify what a change control consists of and recognize the basics of the change control model. Recognize the importance of a change control. ...
Introduction to GMPs
Recognize cGMPs and their importance to the pharmaceutical and medical device manufacturing industry. Identify basic cGMP requirements and the roles ...
Writing and Reviewing SOPs
Identify the rationale and GMP requirements for written SOPs. Recognize which areas require procedures and how those procedures are developed. ...
Understanding Post-Approval Changes
Recognize PAC guidance and how these documents are used to provide notification to FDA for post-approval changes to an approved drug application. ...
Resolving Out Of Specification Test Results
Recognize the possible causes of OOS results. Identify the requirements for handling an investigation of OOS results. Identify how to work with ...
Conducting Annual Product Reviews
Recognize the benefits of conducting an APR. Recognize how to organize an APR. Identify the contents of an APR.
Batch Record Reviews
Recognize the definition of batch records and the purpose of reviews. Recognize the key elements and reasons for organized batch records. Identify ...
GMP Principles of SOPs
Identify what SOPs are, what their purpose is, and how they are structured. Recognize how to handle changes to SOPs as well as how SOPs are used in ...
Awareness of FDA Inspections for Pharmaceutical Manufacturers
Identify the basics of FDA inspections of drug manufacturing facilities, including authority, purpose, types, and the areas/operations typically ...
FDA Training and Qualification Requirements
Identify FDA requirements for personnel training and qualification, responsibilities of personnel, and how to measure training and qualification.
Corrective and Preventive Actions
Recognize applicable regulatory requirements and other important aspects of implementing an effective corrective and preventive actions (CAPA) ...
Pre- and Post-Approval FDA Drug Inspections
Recognize what constitutes a pre- or post-approval inspection. Recognize what possible outcomes may result. Identify some helpful recommendations for ...
Failure Investigations for Pharmaceutical Manufacturers
Identify the failure investigation process. Recognize how GMP regulations address failure investigations and the key components of a good ...
GMP Principles for Batch Records
Identify regulatory requirements and responsibilities for completing batch records. Recognize documentation elements that are required in ...
Handling an FDA Inspection
Recognize the elements of an FDA inspection and your role during the inspection. Identify how an inspection is conducted and how to conduct yourself ...
Meeting GMP Training Requirements
Identify cGMP training requirements as well as other important cGMP training issues, such as types of training, approaches to training, trainer ...
Effectively Responding to FDA 483s and Warning Letters
Recognize the basic principles of FDA 483s and the use of Warning Letters. Recognize the significance of both these documents. Identify the key ...
Vendor Certification for Pharmaceutical Manufacturers
Identify regulator concerns about supply chain quality Recognize new regulations and guidances coming into effect. Identify critical supplier quality ...
GMP Updates: Supply Chain Quality and Emerging Compliance Concerns
Recognize the critical concerns of supply chain quality in the medical device and pharmaceutical industries. Identify the challenges manufacturers ...
Combination Products ÄÂâ cGMP Requirements
Identify the four different types of combination products. Recognize the scope of the new regulation in 21 CFR Part 4, and each of the drug, device, ...
Role of the Qualified Person
Identify the role and responsibilities of both types of QP. Recognize how these fit within EU legislation.
European Union Good Distribution Practices for Medicinal Products
Identify the EU requirements for maintaining product quality and integrity at each stage in the distribution process as defined in Directive ...
Validation of Analytical Laboratory Procedures
Identify applicable regulatory requirements. Recognize the important aspects of analytical methods validation, including the data that must be ...
Data Integrity for Quality Control Laboratories
Recognize the history of data integrity. Identify the types of data integrity issues found by FDA. Recognize possible consequences of data integrity ...
Good Documentation Practices for Medical Device Manufacturers
Recognize the critical importance of creating and maintaining good documents. Identify the stages of the Documentation Life Cycle. Recognize ...
FDA 483s: Inspectional Observations
Recognize the purpose of issuing an FDA 483. Identify what kinds of inspectional observations are included on an FDA 483, when it is issued to the ...
Risk Management in Pharmaceutical Manufacturing
Recognize FDAÂs guidance on risk management and the potential uses and benefits for our industry as a whole.
Pharmaceutical Risk Management: Picking the Right CAPA Tools
Recognize the tools available that can help achieve an effective corrective and preventive actions (CAPA) process.
DEA Compliance
Identify how the DEA enforces the laws and associated regulations under the CSA. Recognize how these regulations complement those of the Food, Drug, ...
How to Meet Drug Retention and Stability Testing Requirements
Recognize the importance of maintaining drug safety and effectiveness over a productÂs shelf life. Recognize basic Principles of Stability and the ...
An Introduction to ISO 13485 - The Quality Management System for Medical Devices
Recognize the difference between ISO 13485 and ISO 9001. Recognize the process approach of ISO 13485. Identify managementÂs role in implementation ...
Principles of Good Documentation
Recognize the importance of good documentation practices. Identify common forms of documentation used during the manufacturing process and the ...
Laboratory Safety
Identify the types of hazards that make a laboratory unsafe. Identify how to prevent or eliminate these hazards through compliance with safety ...
PPE Assessment
Recognize how to perform a workplace hazard assessment for PPE. Identify what hazards to look for. Recognize how to collect and organize assessment ...
Walking and Working Surfaces ÄÂâ Affected Person
Recognize hazards common to walking and working surfaces. Identify how to prevent hazards to walking and working surfaces.
National Patient Safety Goals
Identify standardized credentialing training for HCIRs. Recognize the five substantive training areas recommended for HCIRs. Identify how this ...
Basics of PhRMA Code
Recognize how the PhRMA Code impacts your interactions with healthcare professionals.
Medical Education for Healthcare Professionals
Identify the various types of consulting arrangements that exist between a pharmaceutical company and healthcare professionals and the guidelines ...
Basics of the AdvaMed Code
Recognize how the AdvaMed Code guides your interactions with HCPs.
Reporting Adverse Events for Medical Devices
Identify what a medical device report is and the types of reports that exist. Recognize a companys requirements for reporting adverse events for ...
Massachusetts Pharmaceutical and Medical Device Manufacturer Conduct Regulation (MA Regulation)
Recognize the provisions of the Massachusetts Pharmaceutical and Medical Device Manufacturer Conduct Regulation (MA Regulation), 105 CMR 970.000. ...
MedTech Europe Code of Ethical Business Practice
Recognize the guidelines that apply to the many types of interactions between MedTech Members and HCPs and HCOs. Recognize the importance of ...
Interactions with Healthcare Professionals - In-House
Identify the guidelines, policies, rules, and regulations that govern interactions with healthcare professionals. Identify the appropriate manner in ...
Interactions with Healthcare Professionals - Field
Identify the guidelines, policies, rules, and regulations that govern interactions with healthcare professionals. Recognize the appropriate manner ...
Principles of Cleaning Validation
Identify the basic elements of cleaning validation. Recognize how cleaning procedures are developed, why a cleaning Standard Operating Procedure ...
Collecting Samples and Establishing Limits for Cleaning Validation
Identify advantages and disadvantages of commonly used sampling methods. Recognize the need for established limits of cleanliness in cleaning ...
Documenting Validation Activities
Recognize FDAs definition of validation. Identify the requirements for cGMP compliant documentation of validation processes.
Physician Payment Sunshine Act
Recognize the meaning and purpose of the Physician Payment Sunshine Act. Recognize the definition of key terms and phrases, such as, applicable ...
HIPAA and Privacy Guidelines for Medical Device Sales Representatives
Recognize the basic provisions of the HIPAA Privacy Rule. Recognize how HIPAA affects our detailing and customer support activities. Identify how to ...
Principles of Sterilization
Recognize the definition of sterilization and identify the most common sterilization methods. Recognize the general approaches for validating and ...
Principles of Aseptic Processing
Recognize the general principles and practices necessary to ensure product sterility and safety. Identify the Good Manufacturing Practices (GMP) ...
A Step-by-Step Approach to Process Validation
Recognize the definition of process validation as it relates to pharmaceutical products and medical devices. Identify the steps involved in process ...
Key Concepts of Process Validation
Identify applicable regulatory requirements. Recognize important aspects of process validation. Identify the components of the validation life ...
Data Integrity for Clinical Research Staff
Identify the role of clinical staff in data integrity. Recognize the importance of data integrity and various challenges to data integrity. ...
Review of Basic Statistical Techniques
Recognize how to interpret data using basic statistical techniques. Recognize how to solve technical problems in a straightforward manner and comply ...
A Tour of FDA
Recognize FDAÂs public health mission and how the Agency is organized to carry out its mission. Recognize the history of FDA and the products that ...
Application of GMPs to Analytical Laboratories
Identify cGMP requirements as they apply to analytical laboratory practices. Recognize key concepts related to laboratory documents, raw data, and ...
The Design and Development of Software Used in Automated Process Controls
Identify the SDLC under regulatory requirements for the design, development, and control of software used in automated process controls. Recognize ...
Application of GMPs to Microbiology Laboratories
Identify the importance of handling raw data. Recognize the key approaches for ensuring accurate results. Recognize how to monitor, validate, and ...
Packaging and Labeling of Finished Pharmaceuticals
Recognize GMP requirements for packaging and labeling. Identify the systems and procedures that prevent mix-ups.
ICH GCP Obligations of Investigators Conducting Clinical Trials
Recognize how to comply with GCP guidelines. Identify principal obligations with respect to qualifications and agreements, Institutional Review ...
Introduction to Specialty Pharmacy Management
Identify the major types of specialty pharmacy drugs and how they are administered to patients. Recognize the costs of specialty pharmacy therapies ...
Ethics as the Foundation to Clinical Research
Identify the ethical components of the Nuremberg Code, the Declaration of Helsinki, the Belmont Report, the International Conference on Harmonisation ...
Informed Consent
Identify key historical events that led to the current informed consent regulations and guidelines. Recognize the informed consent process as well ...
The Role of the Clinical Research Coordinator
Identify the CRCs key roles in research and patient protection from pre-study visits through study completion.
Financial Disclosure by Clinical Investigators
Recognize the types of financial arrangements that must be disclosed and the requirements for proper financial disclosure for covered clinical ...
Administrative Roles of the Clinical Research Coordinator
Identify the role of a CRC throughout a clinical trial, as well as recognize applicable Good Clinical Practice standards.
Dietary Supplements -- Packaging, Labeling, Holding, and Distribution
Identify the requirements for dietary supplement product packaging, labeling, holding, and distribution.
Dietary Supplements -- Introduction to Part 111 cGMPs
Recognize the origin and scope of cGMPs for dietary supplements. Identify the purpose of general provisions and personnel subparts as well as the 16 ...
Dietary Supplements -- cGMPS for Manufacturing Plants and Equipment
Identify FDA requirements for manufacturing plants and facilities that produce dietary supplements Identify FDA requirements for sanitation, ...
Dietary Supplements -- Production and Process Control System for Manufacturing Operations
Identify the cGMP process control requirements for manufacturing operations, including sanitation, contamination, rejected products, specifications, ...
Dietary Supplements -- cGMP Requirements for Quality Control
Identify regulatory requirements for Quality Control operations, including material reviews and dispositions. Recognize regulatory requirements for ...
Dietary Supplements -- Requirements for Records and Recordkeeping
Recognize the importance of the Master Manufacturing Record (MMR) and Batch Production Records. Recognize effective documentation practices. ...
Introduction to the Quality System Regulation (QSR)
"Recognize the application of GMPs to the manufacture of medical devices. Identify the components of a quality system. Recognize the elements of ...
Good Clinical Practices (GCPs) for New Product Investigations
Recognize the basic concepts and key elements of GCP, including documentation, purpose, subject protection, and regulatory authority requirements.
Protection of Human Subjects in Clinical Trials
Identify the measures that are in place to protect the rights and welfare of subjects in clinical studies. Recognize informed consent requirements ...
High Purity Water Systems
Identify the typical uses of water in pharmaceutical and medical device manufacturing. Recognize the general process for producing high quality ...
QS Regulation 1: Overview and General Provisions
Recognize the origin and scope of the QS Regulation. Identify the purpose of the Preamble and general requirements of a quality system. Recognize key ...
QS Regulation 2: Quality System Requirements
Recognize the QS Regulation requirements associated with a firmÂs management responsibility, quality auditing, and personnel.
QS Regulation 3: Design Controls
Recognize the design control requirements of the QS Regulation Recognize the terms associated with design controls. Recognize requirements for ...
QS Regulation 4: Document and Purchasing Controls
Recognize the document and purchasing controls requirements of the QS Regulation. Recognize document and purchasing control procedures that ...
QS Regulation 5: Identification and Traceability; Production and Process Controls
Recognize a manufacturerÂs responsibilities relative to the Identification and Traceability, and Production and Process Controls requirements of the ...
QS Regulation 6: Acceptance Activities; Nonconforming Product
Recognize a manufacturerÂs responsibilities relative to the Receiving, In-Process, and Finished Device Acceptance. Identify the Acceptance Status ...
QS Regulation 7: Corrective and Preventive Action
Identify a manufacturers responsibilities relative to the corrective and preventive action requirements of the QS Regulation.
QS Regulation 8: Labeling and Package Control; Handling, Storage, Distribution, and Installation
Recognize a manufacturerÂs responsibilities relative to the labeling, packaging control, handling, storage, distribution, and installation ...
QS Regulation 9: Records
Identify a manufacturerÂs responsibilities relative to the records requirements of the QS Regulation.
QS Regulation 10: Servicing; Statistical Techniques
Recognize a manufacturerÂs responsibilities relative to the servicing and statistical techniques requirements of the QS Regulation.
QS Regulation 11: Application and Inspection of QS Regulation Requirements
Recognize the application and interrelationship of QS Regulation requirements within a medical device manufacturerÂs quality system. Identify the ...
Principles of Auditing
Identify the definition of an audit and the benefits audits provide. Recognize how to develop an audit team and what the team should address during ...
Operating Room Conduct
Recognize elements of the hospital environment and the OR itself. Recognize proper behavior prior to and upon arrival at the hospital. Recognize ...
MDR Regulation 2: Device User Facility, Importer, and Manufacturer Reporting Requirements
Recognize important terms crucial to the device user facility requirements of the MDR regulation. Identify the MDR requirements as they relate to ...
MDR Regulation 3: Requirements for Individual Adverse Event Reports
Identify how user facilities, importers, and manufacturers report adverse events. Recognize the proper forms to use to report adverse events, as ...
MDR Regulation 1: Overview and General Provisions
Identify the key characteristics of the MDR regulation and its preamble as well as the key terms used in the MDR regulation. Recognize to whom the ...
EU In Vitro Diagnostic Regulations (IVDR)
Recognize essential requirements and harmonized standards for in vitro diagnostic medical devices. Identify significant legislative changes made to ...
EU Medical Device Regulation (MDR)
Identify the basic components of the EU Medical Device Regulation. Recognize the definitions and classifications that describe the devices that fall ...
Good Laboratory Practices (GLPs)
Recognize the general characteristics of GLPs. Recognize how GLPs apply to nonclinical studies
Complaint Management for Pharmaceutical Manufacturers
Identify the primary elements in an effective pharmaceutical complaint handling system. Recognize how to document complaint information as required ...
Promotion of Pharmaceutical Products -- In House
Identify the guidelines, rules, and regulations that govern the promotion of prescription drugs. Recognize how these guidelines, rules, and ...
HIPAA and Privacy Guidelines for Pharmaceutical Sales Representatives
Recognize the basic provisions of the HIPAA Privacy Rule. Recognize how HIPAA affects our detailing and customer support activities. Identify how to ...
Promotion of Pharmaceutical Products -- Field Facing
Identify the guidelines, rules, and regulations that govern the promotion of prescription drugs. Recognize how these guidelines, rules, and ...
Enforcement of the Postmarketing Adverse Drug Experience Reporting Regulations
Identify the role of the Postmarketing Adverse Drug Experience Reporting Compliance Program in monitoring and enforcing the drug safety reporting ...
Introduction to the Regulation of Prescription Drug and Biologic Promotions
Recognize how FDA defines promotional materials for prescription drugs and biologics. Recognize the organizations responsible for reviewing those ...
Investigational Product Development
Recognize drug development phases as well as the main purpose of each phase. Recognize how each phase of new product development contributes ...
Q10 Pharmaceutical Quality System
Identify the approach to take in ensuring the pharmaceutical Quality System has the important principles needed to meet regulatory guidance.
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials
Identify the specific requirements of ISO 14155. Recognize the roles and responsibilities of sponsors and monitors in clinical investigations of ...
Import Operations 2: The Process
Identify pre-entry activities, types of entries, and evaluation of entries. Recognize types of import resources, examinations of products and ...
Hazard Communication
Identify hazardous chemical documentation and labeling. Recognize definitions used within HazCom. Identify best practices to use in the workplace ...
Laboratory Specimens for Clinical Research
Identify the rules and regulations that apply to laboratory samples. Recognize how a sponsor utilizes the services of a central laboratory and how a ...
Drug Safety & Adverse Event Reporting
Recognize key historical events that led to the current system of drug safety monitoring, identify the role of pre-clinical testing required as part ...
Import Operations 1: Background
Recognize how FDA ensures that imported products meet US public Health standards. Recognize differences between the regulation of domestic and ...
Benzene
Identify the risks of working with benzene. Recognize methods for monitoring benzene exposure. Recognize practices to prevent fires and spills in the ...
Import Operations 3: Other Activities
Recognize how import filers participate in OASIS. Recognize how FDA identifies and removes violative imports from the US market. Identify how FDA ...
Medical Device Safety Reporting
Identify the regulatory requirements in the medical device clinical trial and postmarketing environments. Recognize device safety monitoring and ...
Fall Protection
Recognize the dangers of all falls. Recognize the greater dangers of falls from height. Recognize fall protection requirements that apply to any ...
Sterile Dosage Forms Introduction
Identify the requirements of sterile products. Identify the methods of aseptic production. Identify the cleanroom requirements.
Selecting and Managing Clinical Contract Research Organizations (CROs)
Identify the requirements for selecting CROs and other service providers. Identify the requirements for effectively managing CROs and other service ...
Ethical Review Boards
Recognize the key events that helped establish the ethical review system. Recognize the membership requirements of an IRB/IEC and the procedures ...
GCP/ICH Obligations of Sponsors, Monitors, and Investigators
Identify the specific obligations of sponsors, monitors, investigators, and their staff in protecting the rights and welfare of human subjects who ...
Implementing an Equipment Qualification Program
Identify the importance of equipment qualification. Recognize the GMP requirements for equipment qualification.
Environmental Control and Monitoring
Recognize the definition of environmental control and environmental monitoring. Recognize how cleanrooms are classified according to International ...
Orientation to GMP Compliance
Recognize regulations and their importance to your industry. Identify basic GMP requirements and your roles and responsibilities for compliance. ...
Handling a Product Recall
Recognize the definition of product recall. Recognize when a product recall is required. Recognize the impact of a product recall on a ...
GxPs
Recognize what practices comprise the GxP regulations. Recognize how these practices relate to each step in the development and manufacture of new ...
Writing Validation Protocols
Identify what validation protocols are. Identify the three types of qualifications and their properties. Recognize the key elements involved in ...
Basics of Cleanroom Operations
Recognize how cleanrooms are designed, validated, and operated.
Recruitment and Retention of Study Patients
Identify acceptable ethical and regulatory recruitment and retention methods that can be used for clinical research trials. Recognize key factors in ...
Aspects of Regulatory History
Recognize the historical events that brought about the regulatory requirements for conducting clinical trials. Identify the standards, ...
Clinical Trial Audits and Consequences of Non-Compliance
Identify the differences between a sponsor site audit and an FDA inspection. Recognize FDA standards for conducting and reporting clinical site ...
Overview of the Clinical Research Process
Identify what is entailed in the research process for new drug, biologic, and device products, including the documents submitted in order to gain ...
HIPAA -- The Impact On Clinical Research
Identify who is required to comply with HIPAA Privacy Rules. Recognize the roles of an institutional review board (IRB) and a privacy board (PB). ...
Obligations of Investigators in Conducting Medical Device Trials
Recognize the requirements for conducting medical device research including following a protocol, safety and reporting standards, and documentation ...
GCP/ICH Obligations of Sponsors and Monitors
Recognize the roles and responsibilities of sponsors and monitors in clinical trials. Identify regulatory requirements, the types of personnel ...
European Union Clinical Trials Directive
Identify the principal elements of the EU Clinical Trials Regulation and Good Clinical Practice Directive.
General Data Protection Regulation
This course covers the European Union’s (EU’s) General Data Protection Regulation (GDPR), which is a harmonized data privacy law across Europe. ...