Pharmaceutical & Biotechnology Training Courses Overview

It’s no secret: the pharmaceutical and biotechnology industries are constantly changing. Keeping track of any and all updates and staying ahead of the competition is difficult. At The Center for Professional Innovation and Education (CfPIE), we offer more than 300 public courses, serving these industries worldwide through customized learning opportunities that keep workers informed of the latest guidelines, regulations and best practices. Explore our biotech and pharma training courses today.

The Benefits of our Pharma & Biotech Training Courses

Our pharmaceutical and biotechnology training courses allow you to:

Improve day-to-day productivity and enhance long-term career prospects.
Our biotechnology and pharmaceutical courses help you stay up to date on evolving regulations, increasing competition, and advancing scientific discoveries with content developed and taught by expert, industry-active instructors.
Satisfy scientific, administrative, regulatory compliance, and marketing needs, with pharmaceutical and biotechnology courses at every level of experience.
Minimize potential problems by training lab, clinical, and manufacturing personnel to industry best practices for improved efficiency and profitability throughout product lifecycles.
Earn valuable pharmaceutical and biotechnology certifications.

Topic Areas Include

Adverse drug events
API specifications
Best practices (GCP, GLP, GMP)
Clinical trials
Drug discovery and development
FDA regulatory compliance
Immunology
Microbiology training
Process validation
Product shelf life
Quality assurance and quality control

ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development Advanced Topics in Biostatistics for Non-Statistician Analytical Method Validation: Biologics & Biopharmaceutical Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Auditing and Qualifying Suppliers and Vendor Best Practices for an Effective Cleaning Validation Program Biostatistics for Non-Statistician Cleanroom Fundamentals: Regulation, Science, Design, Practice, Operation and Management Clinical Document Management: A Trial-by-Trial Compliance Approach Clinical Trial Project Management, Phase 1-4 Best Practices CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Product Computer System Validation Development and Validation of Bioanalytical Assays for Biologic Effective Document Management for Pharma, Biotech & Medical Device

Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries European Regulatory Procedures - EMA and National Requirement FDA Inspections - What Regulators Expect and How to Prepare GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trial GMP Training for the QC Laboratory GMPs for OTC and Cosmetic Products – US and Global Requirements Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirement Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Good Manufacturing Practices Training | GMP Course Implementing an FDA Compliant Stability Program Integration of Risk Management Principles and Activities into the Quality System Introduction to Medical Combination Product Molecular Biology Techniques – Applications in the Biotechnology and Pharmaceutical Industries Introduction to Statistical Analysis of Laboratory Data Laboratory Equipment Validation and Qualification

Lyophilization Technology – Practical Application of the Scientific Principles Marketing & Advertising of Pharmaceutical & Medical Device Pharmaceutical Production Batch Record Review | Training Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Preparation of FDA Submissions and Communicating with the FDA Preparing the CMC Section for NDAs-CTDs-IND Process Validation for Drugs and Biologics Quality Assurance/Quality Control for Biologics and Biopharmaceutical QbD: Product and Process Optimization using Design of Experiments Selecting and Managing CROs Specifications for APIs & Pharmaceutical Drug Product Technical Writing for Pharma, Biotech and Med Device The Drug Development Process - From Concept to Market Writing Effective SOP and Other Process Documents Writing Effective SOP and Other Process Documents

ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development Advanced Topics in Biostatistics for Non-Statistician Adverse Drug Events - Reporting & Regulatory Requirement Analytical Method Validation: Biologics & Biopharmaceutical Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Auditing and Qualifying Suppliers and Vendor Basic GMP Training for the QC Laboratory Best Practices for an Effective Cleaning Validation Program Biostatistics for Non-Statistician Cleanroom Fundamentals: Regulation, Science, Design, Practice, Operation and Management Clinical Document Management: A Trial-by-Trial Compliance Approach Clinical Trial Project Management, Phase 1-4 Best Practices CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Product Computer System Validation Development and Validation of Bioanalytical Assays for Biologic

Effective Document Management for Pharma, Biotech & Medical Device Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries European Regulatory Procedures - EMA and National Requirement European Union Regulatory Issues – New Product Development FDA Inspections: What Regulators Expect and How to Prepare GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trial GMPs for OTC and Cosmetic Products – US and Global Requirements Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirement Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Good Manufacturing Practices Training | GMP Course Implementing an FDA Compliant Stability Program Integration of Risk Management Principles and Activities into the Quality System Introduction to Medical Combination Product Molecular Biology Techniques – Applications in the Biotechnology and Pharmaceutical Industries Introduction to Statistical Analysis of Laboratory Data Laboratory Equipment Validation and Qualification Lyophilization Technology – Practical Application of the Scientific Principles

Marketing & Advertising of Pharmaceutical & Medical Device Pharmaceutical Production Batch Record Review | Training Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Preparation of FDA Submissions and Communicating with the FDA Preparing the CMC Section for MAAs-IMPD Preparing the CMC Section for NDAs-CTDs-IND Process Validation for Drugs and Biologic Quality Assurance/Quality Control for Biologics and Biopharmaceutical QbD: Product and Process Optimization using Design of Experiments Selecting and Managing CRO Specifications for APIs & Pharmaceutical Drug Product Technical Writing for Pharma, Biotech and Med Device The Drug Development Process - From Concept to Market Writing Effective SOP and Other Process Documents US Cosmetic Regulation: FDA CFR Title 21 Training Writing Effective Monitoring Reports and Good Documentation Practices: A Symbiotic Relationship Writing Effective SOP and Other Process Documents

Customized On-Site Training

Many of our robust biotech and pharmaceutical training courses are also available for instruction at your company’s locations. When you choose to pursue in-person biotech training, our staff can adjust your training as we go to suit your staff's needs. We offer custom on-site training to help you satisfy specific disciplines and enhance cross-discipline exposure in a tailored format to best suit your needs.

The customizable nature of our on-site training allows us to integrate training guidelines into real-life scenarios that may have already been a concern in your workplace. These in-person courses encourage participants to engage more with the content, which in turn helps them better retain what they have learned. They are free to ask our instructors questions in real time and get the answers to concerns and scenarios that everyone can benefit from knowing.

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Pharmaceutical & Biotechnology Certification

Since 2001, CfPIE has provided continuing education courses to pharma and biotech industry leaders worldwide. We've connected with professionals in the world's biggest brands and organizations, doing our part to ensure that every employee and volunteer understands the newest developments in their roles and operations. As industry knowledge and regulation adherence become more important than ever for established workers, CfPIE is proud to be a trusted partner in helping your team stay informed and accurate in their work.

Our Certification Program has been utilized by hundreds of pharmaceutical and biotechnology professionals. These industry-recognized pharmaceutical training certifications can help you enhance your credibility and expand your career options – all at no additional cost above standard course fees!

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Connect With Our Training Experts

Your industry requires more expertise and precision than most. Make sure your staff knows everything they need to and can stay up to date with the market's evolution through CfPIE's pharmaceutical training courses. Start your pharmaceutical regulatory training today when you reach out online or call us at 610-648-7550. You can also visit us in person at 128 Pottstown Pike, Chester Springs, PA 19425.

Pharmaceutical & Biotechnology Training Courses Overview

The Benefits of our Pharma & Biotech Training Courses

Topic Areas Include

Customized On-Site Training

Pharmaceutical & Biotechnology Certification

Connect With Our Training Experts

Have Questions?

You will be able to find answers to most frequently asked questions here

Since 2001, CfPIE has:

Check Out Our Life Science Training Courses.

New Title

ABOUT US

USEFUL LINKS

CONTACT US

info@cfpie.com

128 Pottstown Pike
Chester Springs, PA 19425 USA

STAY INFORMED

Your privacy and trust are important to us. We collect your information only for operational and advisory purposes. We do not and will not sell your private information to a 3rd party. By agreeing to this policy, you are giving us permission to contact you about our services and courses.

Pharmaceutical & Biotechnology Training Courses Overview

The Benefits of our Pharma & Biotech Training Courses

Topic Areas Include

Customized On-Site Training

Pharmaceutical & Biotechnology Certification

Connect With Our Training Experts

Have Questions?

You will be able to find answers to most frequently asked questions here

Since 2001, CfPIE has:

Check Out Our Life Science Training Courses.

New Title

ABOUT US

USEFUL LINKS

CONTACT US

info@cfpie.com

128 Pottstown PikeChester Springs, PA 19425 USA

STAY INFORMED

Your privacy and trust are important to us. We collect your information only for operational and advisory purposes. We do not and will not sell your private information to a 3rd party. By agreeing to this policy, you are giving us permission to contact you about our services and courses.

128 Pottstown Pike
Chester Springs, PA 19425 USA