Express Pharma

NOVEMBER 24, 2023

CPHI & PMEC India are anticipated to host over 1500 exhibitors and attract more than 45,000 visitors from over 150+ countries during the three-day event. Notable exhibitors at the event include Dr Reddy’s Laboratories, Biocon, Glenmark Lifesciences, Hetero Labs, ACG, IMA Industria Macchine Automatiche S.P.A,

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Packaging Vaccines Pharmaceutical Manufacturing Hospitals 98

Express Pharma

NOVEMBER 29, 2023

It provides an unparalleled platform for stakeholders to participate in extensive dialogues covering pharma machinery, packaging, analytical instruments, laboratory technologies, equipment, ancillaries, ingredients, and beyond. This curated series of exclusive events aims to captivate industry leaders and experts through diverse formats.

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Packaging Pharmaceutical Manufacturing 110

Express Pharma

OCTOBER 7, 2024

On October 6, 2024, the Federation of Pharma Entrepreneurs (FOPE) and PharmaState Academy conducted Session 6 of the PULSE (Pharma Upgradation & Learning Series for Excellence) initiative, focusing on HVAC Systems and Qualification in pharmaceutical manufacturing. The session began with a keynote address by Thiru M.

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Dosage Pharmaceutical Manufacturing Packaging 96

PharmaState Academy

MARCH 7, 2024

Name Email Phone Number Company Department State City 1 / 15 How does analytics support adherence to regulatory guidelines in the Indian pharmaceutical manufacturing sector? 2 / 15 In the Indian pharmaceutical industry, what does analytics-driven supply chain management primarily focus on?

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Packaging Drug Development Pharmaceutical Manufacturing 64

Quality Matters

AUGUST 3, 2023

They comprise interconnected webs of local and global ingredient suppliers, manufacturers, packagers, distributors, providers, and regulators. active ingredients, excipients, other raw materials) Packaging materials (e.g., Global supply chains are complex and vulnerable to disruption.

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Packaging Compounding Pharmacies Pharmaceutical Manufacturing Documentation 52

GMPSOP

MARCH 30, 2024

211.130 Packaging and labeling operations quotes, – There shall be written procedures designed to ensure that correct labels, labeling, and packaging materials are used for drug products; such written procedures shall be followed. Different products should not be packaged in proximity unless physical segregation exists.

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Labelling Packaging Documentation Pharmaceutical Manufacturing 52

Viseven

SEPTEMBER 14, 2023

For example, a pharmaceutical brand can face increased acquisition costs if a supplier has not delivered on time. It also bears extra replacement expenses when drugs are discarded due to improper packaging. What are the Main Pharmaceutical Procurement Methods?

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Packaging Pharmaceutical Companies Pharmaceutical Companies Dosage 52

GMPSOP

FEBRUARY 25, 2023

Table of Contents Importance of sampling in pharmaceutical industry Pharmaceutical sampling procedures are carried out during and at each major processing step during the manufacturing to ensure the highest quality is attained. These are called primary packaging materials. as their visual aids.

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Labelling Packaging Documentation Pharmaceutical Manufacturing 52

GMPSOP

OCTOBER 28, 2023

The analyst should ensure that the supervisor is notified as soon as an OOS event occurs, the sample is retained, and a documented investigation is commenced. Dealing with out-of-specification results Laboratory result out-of-specification events are a common occurrence in the quality control process.

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Documentation Method Validation Packaging Data Entry 52

GMPSOP

JUNE 28, 2024

Deviations are unusual or unexplained events that can potentially impact product quality, system integrity, or personal safety. Adulterated Pharmaceuticals: 396 warnings iii. Packaging/labeling/Misbranding: 41 warnings vi. Similarly, the packaging, labeling, and misbranding-related warning letters were the top reasons in 2019.

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Documentation Packaging Labelling Pharmaceutical Manufacturing 59

GMPSOP

MARCH 8, 2024

Out of trend results What is the origin of out of specification events? In the early 1990s, the Food and Drug Administration (FDA) inspected a major generic manufacturer in the US and identified concerns with failing test results. The manufacturer challenged the FDA’s view, ending in the US District Court.

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Documentation Dosage Pharmaceutical Manufacturing Packaging 52

GMPSOP

MAY 17, 2024

Sometimes, pharmaceutical manufacturers employ surface profilometry to assess the roughness of stainless-steel equipment. In other areas, such as secondary packaging or material storage areas, the product isn’t directly exposed to the environment, so there is a lower risk of contamination. if used on pre-cleaned surfaces.

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Documentation Packaging Pharmaceutical Manufacturing Compounding 52

GMPSOP

APRIL 3, 2024

A pharmaceutical warehouse is responsible for receiving, storing, and releasing incoming goods (including labeling and packaging) and distributing finished products. These regulations recognize that product quality can be significantly impacted if manufacturing and packaging have taken place.

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Labelling Packaging Documentation Inventory Control 52

GMPSOP

AUGUST 23, 2022

Table of Contents Quality risk management principles are already effectively utilized in many areas of pharmaceuticals manufacturing business. The tool can also be used for any other quality and compliance issues where a risk event is repetitive and a quality decision is urgent.

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Documentation Communication Pharmaceutical Manufacturing Labelling 52

GMPSOP

MARCH 17, 2023

In a packaging line, a printer was used to imprint manufacturing and expiry dates on a batch of empty cartons which will be used to fill tablet strips. Further to corrective action, the defective packaging (carton) lot was destroyed which was initially quarantined. A fresh lot of unprinted cartons was issued for printing.

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Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52

GMPSOP

AUGUST 14, 2023

Packaging lines are fully automated and working without any hiccups. You can also look at the probability of an adverse event and how easily you can detect it. Summary In this post, we have emphasized the importance of performing periodic reviews of validated systems and processes in a pharmaceutical manufacturing environment.

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Documentation Pharmaceutical Manufacturing Packaging 52

GMPSOP

JULY 31, 2023

Pharmaceutical manufacturing operations typically maintain equipment varying from simple balances and scales to complex automated process control and monitoring systems. – High-Speed Tablet/Capsule Counting Machines (Critical for accurate counting and packaging of tablets and capsules).

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Documentation Dosage Labelling Data Entry 52

PharmaShots

FEBRUARY 27, 2023

The theme of the event was Innovation, Advanced Technology, Current Challenges & Opportunities in Pharma & Healthcare Industry under which a series of presentation sessions and panel discussions were held related to pharma trends, APIs, policy reforms, AI, metaverse, current regulatory trends and the direction of pharma and drug discovery.

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Biosimilars Diabetes Packaging Hospitals 40

Pharmaceutical Technology

MARCH 22, 2023

Berden also makes the point that if companies focus their resources on reshoring manufacturing, they may not have the capacity to invest in other pertinent areas such as R&D.“Do The European Commission plans to launch its revised EU pharmaceutical package in Q1 2023 to ease drug shortages,” she says.

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Pharmaceutical Manufacturing Packaging Communication Diabetes 105