pharmaphorum

NOVEMBER 24, 2022

However, with cleanrooms-on-demand representing a feasible and accessible opportunity for those across pharmaceutical manufacturing, what are the key challenges in adoption and how can we expect the industry to overcome them to reap the rewards on offer? But with a single dedicated cleanroom environment costing around $2.5

Pharmaceutical Manufacturing 92

Pharmaceutical Manufacturing Packaging 92

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. billion (Rs 2.1 lakh crores) in the 2022–2023 fiscal year. .”

Packaging 109

Packaging Pharmaceutical Manufacturing 109

Express Pharma

JUNE 5, 2024

Also, the proliferation of antimicrobial resistance (AMR), where overuse of antibiotics leads to resistant bacteria, making infections harder to treat Additionally, pharmaceutical manufacturing consumes substantial amounts of solvents, which are typically highly toxic chemicals, as well as heavy metals.

Pharmaceutical Manufacturing 86

Pharmaceutical Manufacturing Packaging Documentation Compounding 86

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.

Labelling 52

Labelling Packaging Documentation Pharmaceutical Manufacturing 52

GMPSOP

FEBRUARY 28, 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. Checkout sample preview s.

Documentation 98

Documentation Packaging Pharmaceutical Manufacturing Compounding 98

Pharmaceutical Technology

AUGUST 30, 2022

International companies investing in the emerging market of Brazilian pharmaceutical manufacturing will see a higher return on investment than from developed market equivalents, if they choose to compete with local manufacturers to supply Brazil’s growing market and the greater South American region.

Vaccines 78

Vaccines Pharmaceutical Manufacturing Packaging 78

GMPSOP

MAY 26, 2023

– Assessment of packaging and labeling components. computer systems): Make a separate preliminary technical assessment prior to presenting it to the change committee. Change control management for printed packaging artwork Printed packaging components are items where GMP critical information for a medicinal batch is printed.

Documentation 52

Documentation Packaging Communication Customer Service 52

GMPSOP

MAY 26, 2023

– Assessment of packaging and labeling components. computer systems): Make a separate preliminary technical assessment prior to presenting it to the change committee. Change control management for printed packaging artwork Printed packaging components are items where GMP critical information for a medicinal batch is printed.

Documentation 52

Documentation Packaging Communication Customer Service 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. All written and updated by GMP experts.

Documentation 52

Documentation Packaging Pharmaceutical Manufacturing Compounding 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.

Labelling 52

Labelling Packaging Documentation Pharmaceutical Manufacturing 52

GMPSOP

OCTOBER 28, 2023

Packaging material specifications In the pharmaceutical industry, the requirements for pre-printed packaging materials must be well-defined and documented to ensure that you get the items you specified or ordered and that there are no mix-ups. A standard name and a unique item code define packaging materials.

Documentation 52

Documentation Method Validation Packaging Data Entry 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.

Documentation 52

Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52

GMPSOP

MAY 31, 2024

Process validation master plan The process validation master plan accounts for all manufacturing and packaging processes directly employed in the manufacturing and packaging registered products. Following are some examples of validation studies which should be included in the validation master plan: 1.

Documentation 59

Documentation Method Validation Pharmaceutical Companies Pharmaceutical Companies 59

GMPSOP

JULY 31, 2023

We will present the rationale behind the qualification decision and reference that with the GAMP (Good Automated Manufacturing Practice) categories in support of the decision you will make. – High-Speed Tablet/Capsule Counting Machines (Critical for accurate counting and packaging of tablets and capsules).

Documentation 52

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.

Biosimilars 40

Biosimilars Diabetes Packaging Hospitals 40

GMPSOP

JULY 14, 2023

In this article, we will discuss important aspects of equipment cleaning that are required during pharmaceutical manufacturing. In other areas, such as in secondary packaging or in material storage areas, the product isn’t exposed to the environment, so there is a lower risk of contamination.

Documentation 52

Documentation Labelling Pharmaceutical Manufacturing Packaging 52

Pharmaceutical Technology

FEBRUARY 9, 2023

Container Closure Integrity Testing (CCIT) is used to evaluate the ability of a pharmaceutical’s primary packaging to protect the sterility of its contents. On a regular basis, pharmaceutical manufacturers are performing CCIT during commercial production to ensure that packaging processes are operating as they should.

Packaging 52

Packaging Pharmaceutical Manufacturing Communication Pharmaceutical Companies 52

Pharmaceutical Technology

MARCH 22, 2023

You also need to create an attractive climate for the people that you want to have for these kinds of initiatives to want to locate and be present in the European Union.” The European Commission plans to launch its revised EU pharmaceutical package in Q1 2023 to ease drug shortages,” she says.

Pharmaceutical Manufacturing 105

Pharmaceutical Manufacturing Packaging Communication Diabetes 105