“Regulate Your Quality and Manufacturing with Precision.”


Companies that rely on paper-based processes and ineffective manufacturing practices are bound to fail. Take the lead with AEA.

Regulate Your Quality and Manufacturing with Precision.
Automation Engineering & Advisory - Pharmaceutical
Industries

Automation Engineering & Advisory - Pharmaceutical

As the Indian Pharma technology expert as your partner, we aim to deliver a unique offering of integrated solutions, spanning consultancy, inspection, handling, packaging machines and materials, and track and trace.

Industry-leading software, giving Indian Pharma Manufacturers everything they need to unlock the potential of their productivity and business.

what we do

Robotic Process Automation

Electronic Batch Certification

Paper on Glass Advisory & Implementation

ERP Advisory

OUR GOAL

At HSIEC, we help organizations address their toughest challenges, meeting them with sustainable solutions to create lasting value.

Built on strong values, we’re a mission-driven organization. We use our expertise in building powerful systems our clients need to scale, secure and improve their operations with consistency.

No matter how complex your business adversities – we’ve the resources, technology and people operate as one, building positive impacts that matters.

Goals
WHAT WE OFFER
Increased capacity
Increased capacity
  • Reduced production lead time
  • Faster reviewing time from 6-7 days to minutes
Quality Check Assurance
Quality Check Assurance
  • Close to Zero deviation in human error during review
  • Alignment to ISA-95, EMA/INS/MRA/387218/2011 Rev 5
Regulatory Compliance & Review
Regulatory Compliance & Review
  • Accurate batch reporting
  • Country-wise compliance review

Electronic Batch Records (EBR) Software

Achieve compliance and enhance efficiency through the integration of an Electronic Batch Record (EBR) system, automating your paper-based processes.

To meet the regulatory standards outlined in the Current Good Manufacturing Practices (CGMPs), it is essential to provide evidence of proper handling at every stage of the production process. Batch records and various manufacturing documentation serve as tangible proof of this accountability. However, relying on paper-based systems can be laborious and prone to errors. By implementing an appropriate electronic batch record (EBR) software system, the burden of documentation is alleviated for quality and manufacturing teams. Additionally, this system enhances product quality and improves key performance metrics.

Benefits of an EBR Software System

Ensure seamless compliance with regulations.

Track and control production data.

Ensure operational consistency with a single source of truth.

Mitigate the frequency of errors.

The Advantage of Going Paperless with an EBR software

The Advantage of Going Paperless with an EBR software

  • Achieve effortless compliance with regulatory requirements.
  • Establish a streamlined compliance process with ease.
  • Maintain consistent adherence to regulations.
  • Monitor and manage production data effectively.
  • Attain operational consistency through a centralized source of truth.
  • Reduce the occurrence of errors and mitigate their impact.
linkedin post

"The Importance of Good Manufacturing Practices (GMP) and Digitalization in the Indian Pharmaceutical Industry"

linkedin post

“Factors that are deterring companies from pursuing digital transformation in manufacturing”

linkedin post

“Drug Manufacturing Automation: Digital Solutions to Achieve Optimised Precision and Compliance”

OUR EXPERTS

Bidhan Ojha

Bidhan Ojha

Divisional Partner
(15+ years exp.)

Bidhan is the brain behind AEA - Pharmaceutical with an industry experience of over 7 Years.

Let’s Connect

contact us

Follow us