Quality System

Introduction

Our company, Actiza Industry, is determined to provide exceptional quality to all our clients and patients. This proves to be a strong base for our recognition and success on a global level.

The quality system is built in a way that each product and solution we make is potent and safe. We follow stringent global rules regarding quality, maintaining security, efficacy, and regularity.

Our dedication to innovation and in-depth scientific knowledge enables us to consistently produce high-quality formulations in every batch. This earns us trust from many healthcare professionals worldwide.

Our Quality Philosophy

Quality is not just a requirement, but a way of life that guides our people, processes, and partnerships. We encourage all our departments to think Quality First.

Everyone in the company must put quality assurance first before anything. We focus on managing risks before they happen and on making quality better all the time.

We want to build a culture of quality that not only meets but also goes above and beyond international standards.

Quality Assurance (QA) Practices

Our Quality Assurance (QA) team is substantial for keeping our operations honest.

Some essential parts of our QA practices are:

  • Supplier Qualification and Material Assurance :- Only qualified and audited vendors are approved have to meet high standards and be audited. They also get tested on a regular basis. This technique makes sure that they always give you high-quality raw materials and packaging parts.

  • Oversight of Batch Manufacturing :- QA examines each batch by doing Comprehensive batch record reviews. This includes the process, Deviation handling, CAPA implementation, and handling the final procedures.

  • Self-Inspections and Internal Audits :- Regular self-inspections and internal audits ensure that cGMPs are being followed. They also find ways to keep getting better.

  • Following the rules :- QA ensures that all products and processes comply with both national and international laws. This covers guidelines from the US FDA, EU GMP, WHO-GMP, and other relevant regulations.

Quality Control (QC) Infrastructure

Modern labs are part of our Quality Control setup. These labs make sure that all the raw ingredients, intermediates, and finished products follow high-quality standards.

Advanced technologies and machinery make testing more accurate. They make sure that the outcomes are always safe and the best.

Our microbiological labs and environmental monitoring make sure that our products are safe and clean. Before they reach the market, strict sample rules ensure that we meet global standards.

Compliance with Global Standards

Our manufacturing facilities are regularly audited and approved by top global regulators on our production facilities are very severe.

  • Certifications :- Our facilities have been approved by the WHO-GMP, US FDA, EU GMP, and more.

  • Inspections :- We get frequent checks from worldwide health authorities and recognized third-party auditors. This makes sure that our products and systems meet new worldwide requirements.

  • Ongoing Upgrades :- We continually enhance our systems and infrastructure to ensure they meet current Good Manufacturing Practices (cGMP) and future regulatory requirements.

  • Following the rules :- QA ensures that all products and processes comply with both national and international laws. This covers guidelines from the US FDA, EU GMP, WHO-GMP, and other relevant regulations.

Data Integrity & Documentation

Making sure that data is reliable is a key part of our promise of quality:

  • Electronic Systems :- Our reliable electronic systems and secure audit trails keep data safe from anyone who shouldn’t have access to it. They also ensure that everything can be traced in real-time.

  • Controlled Documentation :- Important papers, including SOPs, Master Batch Records, analytical methods, and others, are updated regularly. They are version-controlled, and only people with permission can get to them.

Training & SOP Implementation

The individuals who keep a solid Quality System are what make it strong. We train our teams regularly.

These include cGMP, maintaining data security, staying compliant with new regulations, and acquiring the technological skills required for specific roles.

There are Standard Operating Procedures (SOPs) for every process. These SOPs are developed, reviewed, and revised based on best practices used globally.

Following SOPs makes sure that everything is done the same way, cuts down on mistakes, and makes sure that everything is done right, from buying to packaging.

Certifications

Our systems and facilities hold certifications recognized worldwide. These demonstrate our commitment to the highest standards.

We have the cGMP and WHO-GMP approvals. The US FDA, EU authorities, and other national regulatory bodies have also issued certifications to us.

We have ISO certifications for Quality Management and Environmental Management. These certifications prove that we satisfy high international standards for safety, quality, and environmental responsibility.

Customer-Centric Quality Approach

We care about quality. This is more than merely following the rules. We promise to give every client and patient value and safety.

We always listen to what our customers have to say. We also keep an eye on how well products work with good Pharmacovigilance.

We are proactive about quality. Our swift reaction methods for recalls and complaints help us keep patient safety and customer trust at the top of our list of priorities.

Putting clients first helps us create strong relationships fand keep our good name as a reliable and excellent company.

Request A Call Back