"We provide knowledge and information about CGMP and Quality Systems to the Life Science industry"

Compliance Seminars®

Training session

From Training to Learning
- Improving GMP Performance


Knowledge management is considered a key enabler of a modern pharmaceutical quality system. This workshop provides participants practical ways of how training and learning contribute to a robust knowledge management program, equipping people with the knowledge and skills they need to successfully and safely do their jobs.

Designed as an advanced workshop, this two-day course examines the fundamentals of knowledge management and its practical aspects that contribute to product and process understanding.

Five learning theories are discussed along with how they can be practically used to support performance and create learning programs that are authentic learning opportunities. Participants use concept mapping as a way of reflecting on the topics covered and how they can be incorporated into their own organization.

Goal:

Explore ways of moving from the traditional use of training to where learning, knowledge management, and process understanding contribute to better worker performance, compliant outcomes, and high-quality, pharmaceutical products & medical devices

Course objectives:

  • Distinguish between “training” and “learning.”
  • Describe knowledge management, emphasizing the roles of individual and organizational learning.
  • Develop alternative approaches to knowledge transfer that are grounded in good learning practices and meet regulatory expectations.
  • Identify current expectations that regulatory agencies and auditors have of knowledge management, training systems, programs, and worker performance.
  • Examine models that are used to efficiently design and produce training solutions that meet specific goals.
  • Discuss different models for assessing and evaluating learning and learning programs.

Course outline:

DAY ONE

  • Welcome and introduction
  • What is this stuff called “knowledge”?
  • Tacit versus explicit knowledge
  • Knowledge management and what it includes: the knowledge lifecycle
  • Regulatory expectations for knowledge management and process understanding
  • Moving through the lifecycle: acquiring, analyzing, storing, disseminating
  • Compliance failures and training — identifying the causes
  • Training is not the answer to all your problems
  • Competency-based training
  • A quick look at learning theories: how we learn
  • What qualifies a trainer?
  • What is an expert?

DAY TWO

  • Keys to a successful training system – quick review
  • Assessment and evaluation — how can you measure success?
  • Alignment: Making sure all the pieces fit
  • Organizational learning – what it can mean for the business
  • Beyond training: Other ways to disseminate information
  • Procedures and checklists
  • The connection between training and procedures
  • Other tools that support performance
  • Evidence of training, learning, and performance
  • Evaluating and enhancing YOUR training program

Who should attend:

  • Compliance officers
  • Consultants/service providers
  • Engineering and design controls teams
  • Executive management
  • General/corporate counsel
  • Managers
  • Manufacturing directors and supervisors
  • Medical/technical writers
  • Pharmaceutical and cGMP auditors
  • QA/QC personnel
  • R&D staff
  • Regulatory/legislative affairs professionals
  • Risk management specialists
  • Training personnel
  • Validation specialists, scientists, engineers

 

Gate2GMP®

When attending a Key2Compliance® course, you get access to Gate2GMP®, our document library and search tool.
At Gate2GMP® each course has its own page where you can download course materials, receive up to date information and communicate in the course forum.
Watch this short video to learn more about what Gate2GMP® offers »

 

Bring this course in-house?

Are you a group in need of the same training?
Do you wish to customize this course to suit your needs?

 If so, running the course in-house is probably the best and most cost effective solution.

Make an enquiry

 

 

Register  

 

Course facts

Course no:
5232
Industry:
Pharmaceuticals, Biopharmaceuticals and Medical Device

Level:
Intermediate
GMP region:
US and EU

Language:
English

Date, location and venue:

Prel. May/June 2019, Copenhagen Denmark

This course is also offered in-house.
Click here for more info and inquiry form.


Time:
2 days
8.30-16.30 (Registration 08.00-08.30)

Price (excl. local VAT):
13 780 DKK (€ 1 850) up to 6 weeks before the course
15 280 DKK (€ 2 050) less than 6 weeks before the course

Incl. course material (pdf), lunch and refreshments
Note. Due to tax/VAT regulations within the EU (for courses/seminars/conferences), the course fee is invoiced in the local currency and local VAT is added.
Accommodation is NOT included in the course fee.


Discounts:
For groups registered and invoiced together for the same course we offer the following quantity discount:
2-3 persons 10%
4 or more 20%
Quantity disconts can not be combined with other discounts or offers.
We do not offer or practice any general company discounts without commitments and/or written agreements.

Course material (Handouts)  
No printed course material will be provided on our courses*.
This is primarily to protect the environment. Therefore, we encourage you to bring a laptop / tablet to the course - it is possible to make notes in the PDF file you will have access to.
1-2 weeks prior the course you will receive login details to www.Gate2GMP.com where you can download the course handouts as a PDF.
Note pads and pens will always be provided at the venue.

Cancellation policy - Compliance Seminars®  

Cancellation of registration:

Registration is binding and when you have received our confirmation the following conditions are known and accepted. If you for any reason is unable to attend, substitution is always possible and preferred.
All cancellations and/or substitutions must have been communicated with and confirmed by us.
Cancellations received less than 30 calendar days before course start are subjected to a service charge of 150 € (Euro)/registered course day as compensation for additional administrative burden and for non refundable part of the conference reservation. Cancellations received less than 7 calendar days prior the course, or failure to cancel or "no-show", will be charged in full.

Cancellation of courses: Courses may be cancelled by the organizer if bookings fail to reach minimum numbers (normally not later than 30 days prior the course start), or due to other reasons beyond our control. In such circumstances charged course fees will be refunded, credited, or granted to attend another course for the same value. NOTE! Key2Compliance AB is NOT responsible or liable to any costs in conjunction with a cancelled course. If you need to book flights way ahead (+35 days prior the course) check with us before finalizing the purchase of flights and/or hotel accommodation for an update on the registration situation.