GXP COMPLIANCE THROUGH DIGITAL TRANSFORMATION

 

The pharmaceutical industry is amongst the most dynamic and rapid growth sectors. Compliance and adherence to a wide array of regulatory bodies like USFDA, EMA, and constantly changing regulations are standard.

In order to meet the requirements, the pharma sector needs to integrate quality and compliance into its business processes.

Effective collaborations with software solution providers can enable pharma companies to become agile, streamlined, productive, cost-effective, and aligned to market trends.

At TiMAD IT Solutions, we enable pharma companies to harness the power of digital and technology solutions for automating and digitizing the critical business processes.

TiMAD Digital solutions for GXP Compliance

The rapid pace of acceleration in the pharma sector calls for faster and leaner processes to be compliant and reduce time-to-market.

TiMAD IT Solutions, along with the QualiCultureGxP Consulting Group, is committed to provide a comprehensive software solution portfolio for life sciences industry to address critical business challenges.

Our Value Added Services for the pharma industry:
  • GxP Consulting Services
  • Resource Augmentation
  • Custom Application Development
  • Data Analytics and IoT
Our Transformation Solutions for the pharma industry:
  • Computerzied Maintenance Management Solution
  • Predictive Maintenance using six sigma techniques and IoT
  • Instrument Calibration
  • Intelligent Logbook
  • Laboratory Information and Management Solution
  • Quality Management Solution
  • Stability and Sample Management
  • RFID Enabled Stock Management
  • AI/ML Based Invoice Automation and Contract Management
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Our exclusive specialized expertise

Biotechnological Production

Quality Assurance

Quality Control

Microbiology

Life cycle management of GMP data - Electronic and Hard Copy

Engineering (water systems, HVAC systems)

Pharmaceutical development - Quality by Design

Aseptic / sterile manufacture - Sterility Assurance by Design

Our services are based on the following standards

US FDA

EP/USP

EU EMA

Health Canada

WHO

PDA

ICH

TGA

PIC/S

Japan-MHLW

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