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PROBLEM STATEMENT
Challenges in Manual
Training Process
GMPs mandate that people be taught the GMP requirements that are
applicable to their activities. Each employee has to be trained in the
exact process or operation he/she is involved in. GMP training also
establishes requirements for continuous training and its practical
effectiveness periodically assessed.
Development & implementation of GMP training is time taking
Increasing US FDA observations on Procedure not written & fully followed
Define Learner Roles for Role-based Training
Re-training the employee and re-viewing the procedure
Deploy Training and retraining for published and updated documents
Generate Insight and Take Action based on skills, course completed etc.
Inefficient Competency Assessment
GMP training record retention incurs a huge cost
How
AmpleLogic
Learning
Management
Solution
Enables you
to
Strategies
&
Execute
GMP training
Compliance
Ready
Automates all activities, from distribution of tasks, materials,
and exams to follow-up, tracking, escalation, and verification
Creation of multi-format training content with SCORM
standards including controlled document, videos, image etc.
Provides skill matrix up-to-date view grouped by skill, roles
or department
Revisions in training material (SOPs) can automatically
trigger a notifications and reminder alert to learners
Testing, grading, and documentation of each user’s training
history, with attached training record evidence
Develop your own database of policies, procedures,
assessments, and training to provide measurable results
Tracking Learning Session
COMPLIANCE READY FEATURES
 Formal and Informal Learning
 Classroom and on-the-job
 In person, virtual and digital
 Events or Trainings attended
outside of the organization
Course Versioning and Upgrading
 Track course versions not only in
content but also in prerequisites,
materials, and delivery
 Visibility on which version a
particular learner enrolled
 Course updates automatically
credits the learner to the new
version
 Track courses, programs or
certifications that requires renewal,
and when those renewals need to
occur.
 Reporting engine to create custom
reports to meet unique needs
Reporting Options
A High level Training Flowchart
TRAINING MASTER
Training Material
Training Courses
Course Questionnaire
Course Certification
COURSE ASSIGNMENT
Course Management
Course Group
User Group
Course - User Group Mapping
Nominate for GMP Courses
Job Roles & Responsibility
TRAINING PLANNER
GMP Yearly Training Planner
OJT Yearly Training Planner
Annual & Monthly Calendar
AMPLELOGIC LEARNING MANAGEMENT SYSTEM FEATURE LIST
TRAINING SESSIONS
Self Reading & Classroom Sessions
Practical Sessions
Instructor Led Training (ILT) Session
External Training Classroom Record
Initial / Induction Training
Employee Orientation Program
Auto Scheduling of Sessions
Re-training Session
SNAP Test Module
EMPLOYEE
Learning Path
Self Enrollment
Competency Matrix
To Do List Activities
Job Role / Training Acknowledgement
EVALUATION
Skill Matrix
Employee Training Card
Exam Results
Employee Qualification
Trainer Qualification
REPORTS
Employee Wise Training Completion
Course Applicability Department Wise
Total Training Hours
Department Wise Training Status
GAP Analysis Report
Defaulters Training / Department wise
Course Reports
Initial Training Status Reports
20+ custom reports
WHY AMPLELOGIC ?
Customized Workflow
Role Based Access
Custom Reports and Dashboards
User Permission & Restrictions
Scheduler Configuration
Alert Management
Integration to Quality System
Integration to Active Directory
Biometric Access and Integration
Application Session Management
Login & Password Policy & Checks
Adaptable to Mobile & Tablets
SCORM Standards
Master Data Maintenance
Multi Lingual Content – UI Available
REGULATORY
COMPLIANCE
FEATURES
AmpleLogic solutions are compliant
to meet the requirements of
regulatory bodies like FDA’s 21 CFR
Part 11, EU Annex, MHRA etc.
Audit Trial
Digital / Electronic Signature
Access Authentication
Record Audit
Copies of Records
View History
Solution Integration for coherent business processes
Learning Management System is integrated with key GxP systems providing data to develop enterprise-wide strategy for
learning development. Integration also remove redundant manual efforts that can be time-consuming and automates
some processes. i.e, integration with DMS to support SOP version control and automatic new training creation.
QUALITY SYSTEMS MANUFACTURING SYSTEMS
2010 Operations Started in Hyderabad India
2012 First GMP Implementation of Audit Module using LOW CODE PLATFORM
2014 ISO 9001-2015 Certification
Associated with 10 leading pharma companies for DMS and QMS implementations
Signed up with 7 leading Pharma Companies2015
2016 Recognized by CIO review magazine and Silicon India for unique delivery models
Launched QC automation modules and LMS solution
2017 Associated with 25 US FDA/MHRA/WHO approved Plants
2018 Finalist in CPHI Worldwide Awards, Entry into Egypt and UAE Markets
Foundation to develop new modules like APQR, Product Recall, ANDA & DMF tracker
Started working on draft Quality Metrics guidelines by USFDA
2019 US Market entry, Appreciated by 7 customers during audit on our Paperless automation
120 Young Engineers, 10,000 Sq. feet offices and 3 channel partners
Road map to add more flexibility to eBMR/MES, eLogs
About AmpleLogic
Trusted
by
35+ Pharma
&
20 Non Pharma
Companies across
Globe
Pharmaceutical Business Process - Ready to Use Modules
16 6 6 7 17 1 2
No of Implementations
Yet to Launch
Our Customers
Pharma and Biotech
Non Pharma
Any Queries?
Please Contact us: info@amplelogic.com
Visit Us : https://amplelogic.com/
Thank You

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Strategies for Unlocking Knowledge Management in Microsoft 365 in the Copilot...
 

Learning management system

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  • 2. PROBLEM STATEMENT Challenges in Manual Training Process GMPs mandate that people be taught the GMP requirements that are applicable to their activities. Each employee has to be trained in the exact process or operation he/she is involved in. GMP training also establishes requirements for continuous training and its practical effectiveness periodically assessed. Development & implementation of GMP training is time taking Increasing US FDA observations on Procedure not written & fully followed Define Learner Roles for Role-based Training Re-training the employee and re-viewing the procedure Deploy Training and retraining for published and updated documents Generate Insight and Take Action based on skills, course completed etc. Inefficient Competency Assessment GMP training record retention incurs a huge cost
  • 3. How AmpleLogic Learning Management Solution Enables you to Strategies & Execute GMP training Compliance Ready Automates all activities, from distribution of tasks, materials, and exams to follow-up, tracking, escalation, and verification Creation of multi-format training content with SCORM standards including controlled document, videos, image etc. Provides skill matrix up-to-date view grouped by skill, roles or department Revisions in training material (SOPs) can automatically trigger a notifications and reminder alert to learners Testing, grading, and documentation of each user’s training history, with attached training record evidence Develop your own database of policies, procedures, assessments, and training to provide measurable results
  • 4. Tracking Learning Session COMPLIANCE READY FEATURES  Formal and Informal Learning  Classroom and on-the-job  In person, virtual and digital  Events or Trainings attended outside of the organization Course Versioning and Upgrading  Track course versions not only in content but also in prerequisites, materials, and delivery  Visibility on which version a particular learner enrolled  Course updates automatically credits the learner to the new version  Track courses, programs or certifications that requires renewal, and when those renewals need to occur.  Reporting engine to create custom reports to meet unique needs Reporting Options A High level Training Flowchart
  • 5. TRAINING MASTER Training Material Training Courses Course Questionnaire Course Certification COURSE ASSIGNMENT Course Management Course Group User Group Course - User Group Mapping Nominate for GMP Courses Job Roles & Responsibility TRAINING PLANNER GMP Yearly Training Planner OJT Yearly Training Planner Annual & Monthly Calendar AMPLELOGIC LEARNING MANAGEMENT SYSTEM FEATURE LIST TRAINING SESSIONS Self Reading & Classroom Sessions Practical Sessions Instructor Led Training (ILT) Session External Training Classroom Record Initial / Induction Training Employee Orientation Program Auto Scheduling of Sessions Re-training Session SNAP Test Module EMPLOYEE Learning Path Self Enrollment Competency Matrix To Do List Activities Job Role / Training Acknowledgement EVALUATION Skill Matrix Employee Training Card Exam Results Employee Qualification Trainer Qualification REPORTS Employee Wise Training Completion Course Applicability Department Wise Total Training Hours Department Wise Training Status GAP Analysis Report Defaulters Training / Department wise Course Reports Initial Training Status Reports 20+ custom reports WHY AMPLELOGIC ? Customized Workflow Role Based Access Custom Reports and Dashboards User Permission & Restrictions Scheduler Configuration Alert Management Integration to Quality System Integration to Active Directory Biometric Access and Integration Application Session Management Login & Password Policy & Checks Adaptable to Mobile & Tablets SCORM Standards Master Data Maintenance Multi Lingual Content – UI Available
  • 6. REGULATORY COMPLIANCE FEATURES AmpleLogic solutions are compliant to meet the requirements of regulatory bodies like FDA’s 21 CFR Part 11, EU Annex, MHRA etc. Audit Trial Digital / Electronic Signature Access Authentication Record Audit Copies of Records View History
  • 7. Solution Integration for coherent business processes Learning Management System is integrated with key GxP systems providing data to develop enterprise-wide strategy for learning development. Integration also remove redundant manual efforts that can be time-consuming and automates some processes. i.e, integration with DMS to support SOP version control and automatic new training creation. QUALITY SYSTEMS MANUFACTURING SYSTEMS
  • 8. 2010 Operations Started in Hyderabad India 2012 First GMP Implementation of Audit Module using LOW CODE PLATFORM 2014 ISO 9001-2015 Certification Associated with 10 leading pharma companies for DMS and QMS implementations Signed up with 7 leading Pharma Companies2015 2016 Recognized by CIO review magazine and Silicon India for unique delivery models Launched QC automation modules and LMS solution 2017 Associated with 25 US FDA/MHRA/WHO approved Plants 2018 Finalist in CPHI Worldwide Awards, Entry into Egypt and UAE Markets Foundation to develop new modules like APQR, Product Recall, ANDA & DMF tracker Started working on draft Quality Metrics guidelines by USFDA 2019 US Market entry, Appreciated by 7 customers during audit on our Paperless automation 120 Young Engineers, 10,000 Sq. feet offices and 3 channel partners Road map to add more flexibility to eBMR/MES, eLogs About AmpleLogic Trusted by 35+ Pharma & 20 Non Pharma Companies across Globe
  • 9. Pharmaceutical Business Process - Ready to Use Modules 16 6 6 7 17 1 2 No of Implementations Yet to Launch
  • 10. Our Customers Pharma and Biotech Non Pharma
  • 11. Any Queries? Please Contact us: info@amplelogic.com Visit Us : https://amplelogic.com/ Thank You