Introduction to Cosmetic Science and Ingredients Specialization by

The Pharma Drug Regulatory Affairs (DRA) course equips professionals with essential knowledge and skills for navigating the complex regulatory landscape of the pharmaceutical industry. Covering regulatory guidelines, compliance strategies, and the drug approval process, the course prepares participants to effectively manage submissions, ensure adherence to regulations, and facilitate market access for new and existing drugs. Ideal for those seeking to advance in regulatory roles, it blends theor

Skill Level: All levels

Cosmetics Science

Introduction to Cosmetic Science and Ingredients Specialization

80
[3] days, 8 hour /day
Featured
(Fixed Duration)

This course offers a comprehensive introduction to cosmetic science, focusing on the key ingredients and their roles in product formulation. Participants will explore the basics of cosmetic chemistry, ingredient functionality, and formulation techniques. The curriculum covers regulatory standards, ethical considerations, and emerging trends, equipping learners with foundational knowledge and practical skills essential for the cosmetic industry.

Skill Level: Beginner

Drug Development

Drug Development Product Management Specialization

15
100
Featured
(Fixed Duration)

This specialization delves into drug development and product management, covering the lifecycle from discovery to market launch. Participants will learn about regulatory requirements, project management, clinical trials, and market strategies. The course emphasizes strategic planning, risk management, and cross-functional team collaboration, equipping professionals with the skills needed to successfully manage drug products in a competitive industry.

Skill Level: Beginner

cGMP

An Introduction to ISO 22716 - GMP for Cosmetic Products

50
100
Best Seller
(Fixed Duration)

SO 22716 provides guidelines for Good Manufacturing Practices (GMP) in the cosmetic industry, ensuring product safety, quality, and compliance. It covers production, control, storage, and shipment processes, emphasizing risk management, hygiene, and documentation. The standard aligns with regulatory requirements, helping manufacturers minimize contamination, mix-ups, and errors. Implementing ISO 22716 fosters consumer confidence by ensuring the safety and consistency of cosmetic products globall

Skill Level: Beginner

Pharmaceutical Supply Chain

An Introduction to Pharmaceutical Packaging Training Course

550
100
Best Seller
(Fixed Duration)

The Pharmaceutical Packaging Training Course provides essential knowledge on packaging technologies, materials, and regulations in the pharmaceutical industry. It covers topics such as labeling, tamper-evidence, serialization, and compliance with global standards. This course equips participants with skills to ensure packaging integrity, product safety, and regulatory compliance, making it ideal for professionals seeking to enhance their expertise in pharmaceutical packaging processes.

Skill Level: Beginner

Compliance

Data Integrity and Document Management Training Course

550
100
Free
(Fixed Duration)

The Data Integrity and Document Management Training Course focuses on ensuring accuracy, reliability, and security of data within regulated industries. It covers best practices for maintaining data integrity, managing electronic records, and ensuring compliance with regulatory standards such as FDA and EMA. Participants will learn how to safeguard critical information, implement effective document control systems, and prevent data breaches, ensuring transparency and compliance throughout the dat

Skill Level: Beginner

cGMP

GMP (Good Manufacturing Practice) Fundamentals Training Course

550
100
Free
(Fixed Duration)

The GMP Fundamentals Training Course provides a comprehensive introduction to Good Manufacturing Practice principles essential for ensuring product quality and regulatory compliance in the pharmaceutical, food, and cosmetic industries. It covers key topics such as hygiene, process control, quality assurance, and documentation. Participants will gain practical knowledge on maintaining high manufacturing standards, minimizing risks, and adhering to global GMP regulations. Ideal for professionals s

Skill Level: Beginner

cGMP

An Introduction to Quality Management for Managers Training Course

50
100
Free
(Fixed Duration)

The Introduction to Quality Management for Managers Training Course provides essential insights into quality management systems (QMS) and their role in driving operational excellence. It covers key concepts such as process improvement, performance metrics, compliance, and customer satisfaction. Designed for managers, the course equips participants with tools to implement effective QMS strategies, ensuring continuous improvement, regulatory adherence, and enhanced product or service quality acros

Skill Level: Beginner

Compliance

FDA (Food and Drug Administration) Approval Process for Medical Devices Training Course

50
100
Best Seller
(Fixed Duration)

The FDA Approval Process for Medical Devices Training Course offers a detailed overview of the regulatory pathway for obtaining FDA approval in the U.S. It covers key steps such as device classification, premarket submissions (510(k), PMA), clinical trials, and post-market requirements. Participants will gain valuable insights into navigating regulatory challenges, ensuring compliance, and expediting the approval process for medical devices, making the course ideal for professionals in the medic

Skill Level: Advanced Beginner

Regulatory Affairs

EU (European Union) Pharmaceutical Regulations & Strategy

50
80
Featured
(Self paced)

The EU Pharmaceutical Regulations & Strategy Training Course provides an in-depth understanding of the European Union's regulatory framework for pharmaceuticals. It covers key areas such as drug approval processes, compliance with EMA guidelines, pharmacovigilance, and marketing authorization. Participants will learn strategies to navigate the regulatory landscape, ensuring product safety, market access, and adherence to EU pharmaceutical laws, making it ideal for industry professionals seeking

Skill Level: Advanced

Compliance

Biological Evaluation of Medical Devices

50
50
Highest Rated
(Fixed Duration)

The Biological Evaluation of Medical Devices Training Course provides a comprehensive overview of assessing the biocompatibility and safety of medical devices. It covers ISO 10993 standards, test methods, and risk management strategies to ensure devices are safe for human use. Participants will learn to evaluate materials, conduct biological risk assessments, and ensure compliance with global regulatory requirements, making this course essential for professionals involved in medical device devel

Skill Level: All levels

Clinical Research

Best Practice for Writing Effective SOPs (Standard Operating Procedures)

70
Flexible Online on Demand
Best Seller
(Self paced)

The Best Practice for Writing Effective SOPs Training Course teaches participants how to create clear, concise, and compliant Standard Operating Procedures (SOPs) for regulated industries. It covers structure, formatting, regulatory requirements, and ensuring ease of use. Attendees will gain skills to develop SOPs that enhance operational efficiency, ensure consistency, and meet industry standards, making this course essential for professionals responsible for process documentation and quality m

Skill Level: Beginner

cGMP

CAPA (Corrective and Preventative Action) Training Course

0
500
Highest Rated
(Fixed Duration)

The CAPA (Corrective and Preventative Action) Training Course provides a detailed understanding of identifying, addressing, and preventing quality issues in regulated industries. It covers root cause analysis, risk assessment, and regulatory requirements for CAPA implementation. Participants will learn best practices for creating effective CAPA plans to improve processes, ensure compliance, and prevent recurrence of issues, making it essential for quality and compliance professionals.

Skill Level: Beginner

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