pathwise.com Open in urlscan Pro
160.153.0.32  Public Scan

Form analysis
0 forms found in the DOM

Text Content

 * ePath Online Training
   * ePath Corporate Subscriptions
   * All eLearning Modules
   * Web Based Training for Compliance
     * Current Good Manufacturing Practices- cGMP
     * Quality System Regulation- QSR
     * Good Clinical Practices- GCP
     * Good Documentation Practices- GDP
     * Data Integrity
     * Biologics
     * Combination Products
     * Electronic Records and Signatures
     * ISO 13485
     * ISO 17025
     * EU MDR 2017/745
   * Web Based Training for Quality Systems
     * Intro to Investigations & CAPA
     * Corrective Action or Correction- Which is it?
     * Why Do We Triage?
     * Effectiveness Checks
     * Trending in Root Cause Analysis
     * Intro to Technical Writing Principles
     * Intro to Quality Risk Management
     * Intro to Quality Change Control
     * Intro to Design Control
     * Intro to Human Factors and Performance
     * Inspection Readiness
   * Web Based Training for Regulations
   * Web Based Training for Productivity
     * Effective Meeting Management
     * Microproject Management Web Based Training
   * Webinars
     * Featured Webinar
     * Webinar Memberships
     * On Demand Webinars
 * Accreditation
   * Digital Badges from PathWise
 * Instructor Led Training
   * Investigations and CAPA Training
     * CAPA Training for GCP
     * Role Based Training for Investigations and CAPA
     * Root Cause Investigation Training
     * Effectiveness Checks Training
     * Interviewing Skills Training
     * Quality Event Management Training
     * Conducting Out of Specification (OOS) Investigations Training
     * Complaint Handling Training
   * Technical Writing Principles
     * Documenting Investigations
     * Writing Standard Operating Procedures (SOPs)
     * Writing Validation Documents
     * Writing for Change Control
   * Human Factoring Records Training
   * Quality Risk Management Training
     * Risk Management for Med Device
     * Risk Management for Pharma
     * FMEA Training
     * Fault Tree Analysis (FTA) Training
   * Quality Change Control Training
     * Writing for Change Control
   * Lead Auditor Training
   * Inspection Readiness Training
   * Quality Systems and cGMP
   * Train the Trainer
   * Trainer Certification
     * Certified Trainer FAQ’s
   * Quality System Consulting
     * Remediation
     * Qualification
     * Coaching
 * Client Stories
 * About Us
   * Contact Us
   * White Papers and Help Tools
     * PathWise Partner White Papers and Help Tools
   * Public Training Events
     * Open Enrollment: March 2024
     * Open Enrollment: August 2024
     * Open Enrollment: December 2024
   * PathWise Management Team
   * PathWise Staff
   * PathWise Team of Trainers
   * Careers
   * PathWise Industry News

Select Page
 * ePath Online Training
   * ePath Corporate Subscriptions
   * All eLearning Modules
   * Web Based Training for Compliance
     * Current Good Manufacturing Practices- cGMP
     * Quality System Regulation- QSR
     * Good Clinical Practices- GCP
     * Good Documentation Practices- GDP
     * Data Integrity
     * Biologics
     * Combination Products
     * Electronic Records and Signatures
     * ISO 13485
     * ISO 17025
     * EU MDR 2017/745
   * Web Based Training for Quality Systems
     * Intro to Investigations & CAPA
     * Corrective Action or Correction- Which is it?
     * Why Do We Triage?
     * Effectiveness Checks
     * Trending in Root Cause Analysis
     * Intro to Technical Writing Principles
     * Intro to Quality Risk Management
     * Intro to Quality Change Control
     * Intro to Design Control
     * Intro to Human Factors and Performance
     * Inspection Readiness
   * Web Based Training for Regulations
   * Web Based Training for Productivity
     * Effective Meeting Management
     * Microproject Management Web Based Training
   * Webinars
     * Featured Webinar
     * Webinar Memberships
     * On Demand Webinars
 * Accreditation
   * Digital Badges from PathWise
 * Instructor Led Training
   * Investigations and CAPA Training
     * CAPA Training for GCP
     * Role Based Training for Investigations and CAPA
     * Root Cause Investigation Training
     * Effectiveness Checks Training
     * Interviewing Skills Training
     * Quality Event Management Training
     * Conducting Out of Specification (OOS) Investigations Training
     * Complaint Handling Training
   * Technical Writing Principles
     * Documenting Investigations
     * Writing Standard Operating Procedures (SOPs)
     * Writing Validation Documents
     * Writing for Change Control
   * Human Factoring Records Training
   * Quality Risk Management Training
     * Risk Management for Med Device
     * Risk Management for Pharma
     * FMEA Training
     * Fault Tree Analysis (FTA) Training
   * Quality Change Control Training
     * Writing for Change Control
   * Lead Auditor Training
   * Inspection Readiness Training
   * Quality Systems and cGMP
   * Train the Trainer
   * Trainer Certification
     * Certified Trainer FAQ’s
   * Quality System Consulting
     * Remediation
     * Qualification
     * Coaching
 * Client Stories
 * About Us
   * Contact Us
   * White Papers and Help Tools
     * PathWise Partner White Papers and Help Tools
   * Public Training Events
     * Open Enrollment: March 2024
     * Open Enrollment: August 2024
     * Open Enrollment: December 2024
   * PathWise Management Team
   * PathWise Staff
   * PathWise Team of Trainers
   * Careers
   * PathWise Industry News


COMPLIANT. EFFECTIVE. EFFICIENT.

Virtual Instructor Led Training.

PathWise is the leading, global provider of quality systems solutions. We
partner with life science organizations to ensure quality, safety and compliance
in our world’s healthcare.

View a Demo, Get a Quote!


EPATH ONLINE TRAINING

Our interactive, informative modules ensure your employees are up to date on the
laws and regulations that govern our regulated life science industry.

View a Demo, Get a Quote!


VIRTUAL INSTRUCTOR LED TRAINING

Our training is interactive, with case studies, group work, and dialouge between
the instructor and learners. Done virtually, it can be cost effective for your
organization, and safe for your employees. 

Get a Quote!


EPATH ONLINE TRAINING FOR LIFE SCIENCES

ePath modules are self led, and interactive. Learning checks along the way
ensure learners are actually retaining information, and not just clicking
through slides. 

View a Demo!


QUALITY SYSTEMS AND COMPLIANCE

We deliver the methodology and tools to ensure compliant, effective and
efficient execution of quality system requirements. 

View a Demo, Get a Quote!


ONLINE TRAINING FOR COMPLIANCE

PathWise strives for excellence and quality in all that we endeavor and keep
up-to-date with applicable regulations and emerging industry trends, bringing an
intimate knowledge of regulatory and compliance standards.

View a Demo!


WEBINARS

PathWise Webinars are the solution for individuals including management,
engineers, regulatory and QA/QC professionals in need of training but unable to
make a full course time commitment. Webinars include on-demand or live
presentations covering various quality system topics. 

Memberships Available!


TRAINING SOLUTIONS FOR OUR WORLD'S HEALTHCARE

PathWise is the leading, global provider of quality systems solutions. We
partner with life science organizations to ensure quality, safety and compliance
in our world’s healthcare.

View a Demo, Get a Quote!


EARN CEU CREDIT!

Continuing Education Units (CEUs) are nationally recognized by a wide range of
organizations, including professional associations, regulatory boards,
corporations and universities. Organizations such as ASQ require a certain
number of CEU for certification. PathWise offers CEU credit for online and
instructor led courses!

PreviousNext
123456789


COMPLIANT. EFFECTIVE. EFFICIENT.

 In a globally regulated life science industry, PathWise provides proven
methodologies in quality and compliance through hands-on and practical solutions
that ensure compliant, effective, and efficient quality systems. Through virtual
instructor led and on-demand online modules, we help simplify necessary concepts
and processes, ensuring a quality system program that conforms to industry and
regulatory standards.



 




INSTRUCTOR LED VIRTUAL TRAINING

PathWise instructor led training allows feedback & dialogue between the attendee
and instructor, while working through problems in the safety of the classroom
environment. Our virtual training environment has the same interactivity and
engagement as the classroom, with the safety of learners participating from
their homes. 



ONLINE TRAINING THROUGH EPATH

PathWise online learning allows for training flexibility, teaching rules,
definitions, and regulation requirements. The self led modules include
interactive learning checks, and helpful downloads and tools to support your
quality system needs.    

MEDICAL DEVICE

Full understanding and compliance with the Quality System Regulation (QSR) is
key for your organizations success. Whether it is CAPA training, supplier
auditing, or any other quality system need, PathWise has the experience to help.

PHARMA

Developing a systematic, compliant approach to current Good Manufacturing
Practices (cGMP) and 21 CFR parts 210 & 211 isn’t easy. PathWise provides tools,
systems, and best practices to simplify regulatory compliance for Pharmaceutical
companies.

BIOLOGIC

Biologic and biotechnology regulations are becoming increasingly rigid, and
having the right support to understand and comply with 21 CFR parts 600, 601,
and 610 can make all the difference. 

FROM OUR LEARNERS


INVESTIGATIONS AND CAPA

“It really helped me sharpen my problem solving brain. Now I can use the tools I
learned to more effectively investigate issues.”

-Dan Eccles, Technician, Takeda

 


INVESTIGATIONS AND CAPA

“This course was one of the best if not the best that I have participated in. I
have been using the skills that I learned and truly believe that they make a
difference.”

-Hans Willems, Quality Director, Bristol-Myers Squibb


TECHNICAL WRITING PRINCIPLES

 

“The variety of examples [were helpful], and despite being ~8 hours the class
was engaging and fun because of the instructor.”

-Lucas Von Samson, Scientist, Abbvie


TECHNICAL WRITING PRINCIPLES

“It was beneficial to have hands on activities that illustrate the points being
discussed. You always hear about filler words, but its much easier to understand
with examples!”

-Brian McDonald, Scientist, AbbVie


TECHNICAL WRITING PRINCIPLES

“The breakdown of academic, technical and literary writing styles was
eye-opening. It was beneficial to perform activities to shorten words,
de-clutter, and re-write documents. It was very beneficial to use real-life
examples and documents used within Lonza to demonstrate dos and donts of
technical writing. It was also beneficial to treat this course as an open
discussion platform. “

-Margaret Chaney, Lonza


INVESTIGATIONS AND CAPA

“After receiving training through PathWise, we certainly see a general
improvement in our CAPA process, including Root Cause Analysis and
Documentation. There is also a reduction in the number of open CAPAs, resulting
in less people being involved and less pressure for our organization.”

-Hans Willems, VP Operations, Boston Scientific


INVESTIGATIONS AND CAPA

“I have been doing CAPA’s for 19 years, but never like this – great tools and
presentation to help understand processes better to take back and add to our
company’s process. ”

-Kimberly Bulls, Regulatory Affairs/Compliance Specialist, Techlab, Inc.


INVESTIGATIONS AND CAPA

“The exercises that went along with the implementation of the concepts and tools
were beneficial – there is nothing better than having people in a training
session actually putting the concepts into practice and using the tools – people
learn much better by doing than by sitting and listening all day. ”

-Patti Skeens, Tesaro




QUALITY RISK MANAGEMENT

“I would refer this course to others. It was a perfect introduction into Quality
Risk Management. It covered the fundamentals and allowed the attendees to work
together testing their knowledge of Risk Management. Those that attended now
have an understanding of what is required for Risk Management. They are now
empowered to be an active participant in Risk Management instead of passively
filling out fields in a template.”

-Desiree Davis, Merge Healthcare


QUALITY RISK MANAGEMENT

“It brought together people from diverse functions (development, manufacturing,
regulatory, customer care) and gave us a common risk language and a forum to
discuss and understand risk management. The course was an appropriate mix of
presentation and student dialog facilitation.”

-Jeffrey Stevens, Roche


QUALITY RISK MANAGEMENT

“Case studies that help apply conceptual tools into an actual process that can
be translated andapplied to work related activities [were helpful]. Yes, a good
introduction courseregarding risk management and tools to use in defining
possible risks.”

-James Chi, Systems Engineer, Hologic



“I enjoyed learning and having the ability to complete activies within the
booklets at the same time. It made understanding the concepts easier and more
enjoyable. I honestly thought all of the content was beneficial.”

-Megan Carter, Lab Technician, Siemens Healthcare

“It was beneficial that the course used a lot of examples that related to our
company it made it a lot easier to relate and understand. It was also helpful
working outloud in small groups. A lot of individuals in the course worked in
different departments and were at different levels and therefore everyone had a
different thought of a different process in the way they worked through a
problem.”

-Emily Muyleart, Production Chemist, Immucor

“The trainer was knowledgeable and engaging. They limited the PowerPoint Time
and Maximized the Team/Group work – key for learning and participant
engagement.”

-Derek Sanders, Director of Supply Chain, Immucor

PreviousNext
1234567891011121314



QUALITY SYSTEMS AND COMPLIANCE TRAINING SOLUTIONS. 



For over 20 years PathWise has delivered superior training, to simplify
necessary concepts and processes in your quality systems. 


EPATH USERS


INSTRUCTOR LED LEARNERS TRAINED ANNUALLY


ONLINE TRAINING COURSE TITLES


VIRTUAL INSTRUCTOR LED COURSE TITLES


COUNTRIES TRAINED FOR


EARN CONTINUING EDUCATION CREDIT

 PathWise is accredited by the International Association for Continuing
Education and Training (IACET).  PathWise complies with the ANSI/IACET Standard,
which is recognized internationally as a standard of excellence in instructional
practices. As a result of this accreditation, PathWise is accredited to issue
the IACET CEU.

Learn More

COMPANIES WHo choose pathwise

PathWise has trained and supported some of the top organizations in the Life
Science industry.



LEARN MORE

 * PathWise White Papers
 * About Us
 * PathWise Management Team
 * PathWise Staff
 * PathWise Team of Trainers

FOLLOW US!

     

TERMS OF USE

Terms of Service Agreement

Privacy Policy

©PathWise 2022

 

CONTACT US