For development of Therapeutics, Devices & Diagnostics

Customized Training

Custom Training (On-Site)

Our customized on-site training program allows organisations to experience the same in-depth, quality content delivered by industry-active experts in the convenience of their own offices. Whether you are training new hires, preparing for an regulatory audit, or updating current personnel on industry or product changes, on-site training courses are ideal.

Program Overview

  • Available for groups of 10 or more
  • Same instructors as classroom courses – they bring the top content formats to you
  • Flexible dates and scheduling options
  • Certification Programs also available through on-site option

On-Site Training Benefits

  • Industry-active instructors promote dynamic learning
  • 80 courses to improve skills, stay up-to-date, improve productivity
  • Certification at no additional cost above standard course fees
  • Group training tailored to company-specific needs

Cost Savings

  • Save money on travel expenses for multiple employees
  • Alternative to internal staff – utilize our affordable industry experts and pay only as needed

Time Savings

  • Avoid having one or multiple staff members spending time traveling
  • Flexible scheduling allows you to dedicate time according to your schedule

Customized Content

  • Courses are formatted around your company’s specific needs and objectives
  • Quickly address issues of immediate concern to your company, i.e. regulatory audits

Consistent Attendee Experience

  • Employees receive same current knowledge in identical frame of reference
  • Foster communication amongst internal teams with industry-active experts adding discussion value

Sl Training Program
1 Writing Effective Standard Operating Procedures and Other Process Documents
2 Indian Regulatory Procedures – Comprehensive Overview of CDSCO and National Requirements
3 The Drug Development Process – From Discovery to Commercialization
4 Selecting and Managing CROs
5 Validation of Computer Systems
6 Biostatistics for Non-Statisticians
7 Good Clinical Practices (GCP) – Understanding and Implementing the Current Global Requirements
8 Adverse Drug Events – Reporting & Regulatory Requirements
9 Good Laboratory Practices (GLP) for Pre-Clinical Testing
10 Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices
11 Project and Program Management for enhanced productivity
12 Product Labelling for Regulatory Products
13 Process Identification, Mapping and Improvement
14 IT Systems & Data Integrity
15 Essential Regulatory Documents Creation and Management
16 Process Identification, Mapping and Improvement
17 Import and Marketing
18 Product Recall Management

Discuss Your Needs

Thank you for your interest in Vyomus Consulting. To conact us, please complete the form below or send us email at info@vyomusconsulting.com

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