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What is PROFISOL ?

IT Provides full-spectrum of services to Formulation / API / Bulk-drug / R&D Pharma companies. 

Pharmaceutical industry is facing challenges in executing regulatory processes, Auditing Reports Generation and Experience Human Errors. The solution includes task reminders intrinsic to large projects that has long gestation. The task reminder helps in completing the project to deadlines and manage cost effectively. The solution is built to reduce production cost as well as efficient resource utilization.

ProfiSol captures comprehensive process flow for production divisions of Pharma organization. These are with built-in cGMP FDA, 21 CFR Part II practices by product life-cycle while such compliance considered as prime and basic requisite for Pharma. With such solutions, it would be simple to manage your business more efficiently. ProfiSol makes the production of batch processing simple and it enforces compliance to standards, any adjustments to defined standards are executed with proper tracking and approvals.

What we offer

· We offer IT products best in market when compared to features
· We offer competitive pricing for our products and any customisation based on your requirement.
· We offer competitive pricing for any IT services and custom IT Project development.
· Solution for any business case

HIERARCHY OF OUR PRODUCT:

Profisol (Complete Pharma solution, will be customised for other domains)

  • CRM/Sales - Marketing(Target, Leads, Contacts, Accounts..), Sales(Leads, Contacts, Accounts, Opportunity, Quotation..), Support(Contacts, Accounts..), Mobile Apps, Reports
  • Warehouse/Store - Stock management, stock availability reports and other
  • eLearning - Training, Annual calendars, tracking attendees/unattendies and other)
  • HR - User Profile, Attendance, Payroll, Appraisal, other
  • Finance - Payment / receipts intimations and remainders, balance sheet, integrated to Procurement/Sales/Payroll
  • Production – eBMR, Templates for each FP, BOM, Serialization, Cross checking resource availability, Production planning & Scheduling
  • QA / QC - Test results, approvals and others
  • Change Management - Change Request, create committee for a request and assign tasks, track the progress of completion
  • Asset Management (OQ, PQ)
  • Environment Monitoring - Microbiology tests planning and scheduling
  • RA - Licenses received for a product to a country, and other
  • Administration - Users creation, configuration

Special Features

  • QR Codes for materials
  • Container / Material tracking with BLE (Blue Tooth Low Energy) technology (in premises), Mobile sim (Out of premises)
  • Digital Signatures
  • Document scanning and auto up loads using mobile
  • Mobile Apps

EasyLab (Pharma R&D)
Automates the research process(re-formulation) in any pharma Labs where huge testing with varied test parameters is involved, presentation for the same in the attachment.

This application is well suited for Lab where analysis is carried out in complex environments and varied time periods. This application tracks the complete flow of the project from the stage of initiation by giving a formula to test till the result of analysis. 
Working on this application including following modules and we will be delivering in 4months.

  • FD – Formulation Department
  • AD – Analytical Department
  • QA – Quality Assurance
  • Warehouse/Store
  • Calibration
  • Dispose
  • Reports
  • Administration

Work flow and authentication in each level and most of the manual process is automated including the formula generation, mean calculation and other, this system is currently not integrated with the lab equipment, we can do the same on the need basis.

We developed our product based on following below required Pharmaceutical Quality Manufacturing standards.

1. 21CFR Part 11

2. CGMP standard implementation in production, can customise it as per requirement

3. Reporting as per audit requirements with Date and time can be tracked if required (Customisable reporting)

4. Maintain complete historical data (Will archive past data based on company standards)

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