Ready-built · Configurable · Proven

Our Accelerators

Ready-built, configurable solutions that shorten implementation time for Pharma and Manufacturing teams.

Each accelerator is a proven starting point, not a blank project. They cover regulated pharma needs such as computer system validation, 21 CFR Part 11 logbooks, DMF and CAPA, and manufacturing needs from procurement and shop floor to finance.

27Ready-built accelerators
2Industries: Pharma & Manufacturing
WeeksTo go live, instead of months
Built in on every accelerator
  • Single sign-on
  • Role-based access
  • Audit trails
  • Central approvals
  • 21 CFR Part 11 ready

Pharma & Life Sciences Accelerators

Compliance-ready solutions for regulated labs, plants and quality teams.

Budgeting & Asset Management

Digital Work Permit

Instrument Access & Booking

Digital Logbook

Computer System Validation

CSV

Abbreviated New Drug Application

ANDA

Drug Master File

DMF

RCA, CAPA & Deviation

Healthcare Professional Management

HCP

Clinical Publication Request

CPR

Deficiency & Open Issues Management

DIMS

Integrated Library of Harmonised Health-Based Values

ILHV

Sample Management

SOP Document Management

Smart ChatBot

Regulatory Affairs

RA

Electronic Lab Notebook

ELN

Project Portfolio Management

PPM

Manufacturing Accelerators

Digitise procurement, shop floor, finance and documentation end to end.

Manufacturing ERP Framework

Vendor Management

Electronic Request for Quotation

e-RFQ

Back-to-Back Costing

Domestic Value Addition Certificate

DVA

Applicator Automation

Accounts Payable & Receivable Automation

AP / AR

Document Management System

DMS

Manufacturing ChatBot

One common platform

Every accelerator shares the same foundation, so they work together from day one.

  • Single Sign-On
  • Centralised master data
  • No duplicate data
  • Dynamic delegation of authority
  • Central approvals
  • Central notifications
  • Centralised user access