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How prepared are we? By Anil Arora Turning the vision of a future-ready pharmaceutical manufacturing facility into reality is no

CMO Quality Management Insights By Londa Ritchey The pharmaceutical industry and the creation of new drugs is expected to continue

Impressions – Customers, Partners & Vendors Listening to You – Customer Speaks Hafeezur Rehman – Senior Vice President (Facilities, Engineering

The Core of Parle Rajamani RamanathanCOO & Director During my 26-year tenure at Parle Global Technologies, I had the privilege

Performance Analysis of Quality-Centric, Novel, Hard-Gelatin Capsule Filling Machine This article outlines the performance superiority on an innovative engineering concept

What does GRANUREX® do? By far, the GRANUREX® is the most powerful pellet/powder processor available in the market place. The

“Our vision is to be a global leader in providing innovative, sustainable, and technology-driven solutions across the Pharmaceutical, F&B, Cosmetics,

Mr. Rajmal L. Mehta, the visionary founder, who transformed Parle Global Technologies into a trusted name globally, offering high-quality machinery,

The Key to Formulation Development During the tablet manufacturing process, tooling and press manufacturers are often faced with ongoing challenges.

Artificial Intelligence (AI) is an emerging technology-driven tool to support various processes from Design & Development to Distribution & Delivery

Portfolio Management may be the most important, misunderstood, and underappreciated function in pharma. No one questions the purpose of Quality

Radio Frequency Identification (RFID) refers to a wireless system comprised of two components: Tags and Readers. An RFID tag is

In this article, the author shares his experience with different validation models. The validation is widely accepted in the life

By Olena Chervonenko Each organisation is responsible for ensuring their vendors provide consistent quality of services and materials which are

Conventional Training Vs Virtual Reality (VR) training Why Pharma Industry Need to Look Beyond Conventional Training? By Subrata Chakraborty The

Cleanroom Validation Ensuring Quality and Compliance in Controlled Environments By Pradip Bhalerao Cleanroom validation plays a pivotal role in industries

Why training is important There are 2 reasons why training is important. The first is a GMP regulatory requirement [21CFR

Good Powder Flow Is Everything! By Fred Rowley On a tablet press or encapsulator, good powder flow is everything! It

Rajni Jha (an IIT Kanpur Scholar), Ex Vice President Regulatory Affairs, is a senior  pharmaceutical regulatory, quality and compliance professional with

Those who are involved in the aseptic manufacturing, injectable manufacturing, sterile product manufacturing, must be aware that media fill is

Offering new impulses for the process industry At ACHEMA 2022, the world’s leading trade show for the process industry, over

By Dr. Tim Sandle  An important objective of hygienic design relating to the pharmaceutical and healthcare sectors is with the

In this exclusive on Cleaning Validation by Pharma Machines & Technology, Igor Gorsky, a pharmaceutical industry global expert, writes on

Globally recognized digitalization and innovation enabler, Antares Vision Group offers full stack of traceability and serialization solution, from machines till

The Antares Vision story begins in 2007 when Emidio Zorzella and Massimo Bonardi, friends since the university years at the

Antares Vision Group in India – Past, Present & Future’ Antares Vision India Pvt Ltd., 100% subsidiary of Antares Vision

TRACK & TRACE Antares Vision Group innovative Track & Trace solutions use advanced technologies to guarantee the whereabouts of each

Portfolio management as we know it today in the generic pharma industry is a relatively new discipline. The term was

Natoli Engineering Inc, USA, conducted a training program on tablet compression at Bombay College of Pharmacy on 21st May 2022,

Q1. Why is QRM important for a pharmaceutical organization? Quality Risk Management (QRM) is important as it ensures that we

For quality inspectors also, it’s a core area of interest to confirm its compliance during regulatory audits to ensure that

By Dr. Tim Sandle Advances in biotechnology have led to a new generation of vaccine treatments entering development and trial.

Area Qualification When we have designed our area for the cleanroom operations, we have to prove that it is maintaining

We have to prove that laminar airflow is maintained in the filling machine while we are doing various activities in

Dhavalkumar Surti, an expert in aseptic techniques, continues to share his knowledge and core experience in the pharmaceutical industry. Here

A documented and approved disinfection programme must be designed, validated, and implemented as part of any pharmaceutical manufacturing area certification.

By: Manish Agarwal The world is facing its toughest challenge due to the current pandemic and just as we have

By: Varadharaj Vijayakumar This article describes the hold time expectation for the partially stoppered media filled vials during validation of

Isolators in Aseptic Processing By Varadharaj Vijayakumar This article describes the basic concepts of isolators, type of isolators in pharmaceutical

I, Masih Jaigirdar, by education am a Pharmacist and by profession a Pharmaceutical Scientist started my professional career in the

While choosing Packaging as career 34 years back (1985), I was not fully aware about its role and importance in

The Covid-19 pandemic has disrupted the manufacturing of biopharmaceutical products due to uncertainty in the supply of raw materials, excipients,

In our daily life we see and use many products since leaving the bed in the morning, till we take

Robotics in Pharmaceuticals – to address safety and contamination concerns The need of the pharma industry today is much higher

Automation does not always result in success, and poor automation can be as damaging to the pharmaceutical organization as no

Aseptic processing can be defined as the processing and packaging of a commercially sterile product into sterilised containers followed by

Introduction Many pharmaceutical companies embrace automation and other digital-based technologies such as those connected to data-driven decision-making to create process

1. They Accelerate the Drug Discovery Process While the word “robot” conjures up images of physical machines, not all robotics

SOPs 10-15 YEARS BACK If we go back approx. 10-15 years, the writing of SOP’s was compact. Employee can complete

STANDARD OPERATING PROCEDURE, popularly known as SOP, is probably an essential document in the pharmaceutical industry and the most neglected

The world has in the last one year, witnessed the biggest disruption unprecedented in history. The pandemic has made a

Survey Report on Virtual FAT Conducted in Pharmaceutical Industry A survey was conducted on Virtual FAT (Factory Test Acceptance) in

Onsite Factory Acceptance Test Vs Virtual Factory Acceptance Test Based on survey report on “Virtual Factory Acceptance Test” in pharmaceutical

Robust Documentation easy on remote Installation Mr. Patel shared his experience of how the customer, with the support of perfect

“Every person engaged in the production, processing, packaging, or holding of pharmaceuticals shall have education, training, and experience, or any

Pandemic Fallout – Role of Indian Pharma – Digital Impact & AI The current pandemic which the world has been

COVID-19 A Great Opportunity: INDIAN PHARMA 2020-2030 Indian pharmaceutical industry aspires to become the world’s largest supplier of drugs by