European Pharmaceutical Review

AUGUST 23, 2024

In this blog , a summary of the key changes of relevance to primary packaging components and how West can help with the implementation will be discussed. Read more The post Are we set for the revised EU GMP Annex 1? appeared first on European Pharmaceutical Review.

Packaging 72

Packaging 72

Fuld & Company Blog

SEPTEMBER 11, 2024

When launching a new product, revamping a marketing strategy, or aiming to build stronger customer loyalty, neuromarketing can help businesses: Understand consumer behavior on a deeper level Refine marketing strategies based on real, emotional responses Optimize product design and packaging to appeal to unconscious preferences Create campaigns that (..)

Packaging 52

Packaging 52

Express Pharma

JANUARY 17, 2025

The company focuses on utilising packaging to minimise end-of-life waste and employs distribution methods that further reduce environmental impact. Downstream Activities (Scope 3) Lonza has designed optimised distribution networks to reduce transport distances to customers, ensuring efficient logistics with a lower carbon footprint.

Dosage 104

Dosage Pharmaceutical Manufacturing Packaging Drug Development 104

Express Pharma

FEBRUARY 7, 2024

Sustainable packaging for parenteral medicines Traditionally, the packaging of pharmaceutical products, especially in the parenteral medicine sector, has been resource intensive. The industry is transitioning towards materials that prioritize the planet – opting for biodegradable, recyclable, and smarter alternatives.

Packaging 104

Packaging Communication 104

Express Pharma

MARCH 18, 2024

Driving environmental innovation: Green chemistry, waste management, and sustainable packaging in pharma In the quest for a greener future, pharma companies are embracing innovative strategies to minimise their environmental footprint. Furthermore, the development of eco-friendly packaging is gaining momentum.

Packaging 105

Packaging 105

FDA Law Blog: Biosimilars

JULY 22, 2024

FDA Law Blog readers receive a 10% discount off the tuition fee (promo code D10-999-FDA25 ). s John W.M. Claud will be speaking at the conference in a session titled “Crafting Your Safety Blueprint for Adverse Events and Recalls under MoCRA.” You can register for the conference here.

Packaging 59

Packaging Labelling 59

Express Pharma

APRIL 5, 2024

Therefore, in order to produce superior quality products, it is imperative to provide high-quality air, devoid of even the slightest trace of moisture for various stages of pharma processes entailing manufacturing, storage, research, testing, and packaging.

Packaging 95

Packaging 95

Board Vitals - Pharmacist

DECEMBER 21, 2022

Effective January 3, 2023, BoardVitals is discontinuing its CME Pro Plus package. The post An Update on BoardVitals CME Pro Plus appeared first on BoardVitals Blog. This decision aligns with our core values, primarily trust and transparency with our customers. CME Pro Plus will simply no longer exist as an option for purchase.

Packaging 52

Packaging 52

pharmaphorum

OCTOBER 27, 2022

Blogs – A company is free to own a blog or engage a blog writer by way of sponsorship or consultancy fees. In the EU and UK, where direct-to-consumer promotion of POMs is prohibited, companies may not sponsor blogs that promote, or could reasonably be expected to promote, such products.

Communication 98

Communication Pharmaceutical Manufacturing Packaging Documentation 98

Putting Patients First Blog

JULY 22, 2024

There is hope that several of these proposals could be put into one larger health care package and passed during the lame duck session. Health Care Legislation There have been ongoing negotiations throughout the year about a slew of health care policy proposals.

Packaging 59

Packaging 59

FDA Law Blog: Biosimilars

JUNE 26, 2024

eSTAR Templates As we have previously explained in our blog post here , eSTAR is an interactive PDF form designed to assist users in creating “complete” submissions. package labeling is optional). It includes questions about the product, that when answered, reveal additional information that should be supplied with a submission.

Labelling 98

Labelling Packaging 98

Pharma and Life Sciences Blog

NOVEMBER 18, 2024

Explore the report Executive Summary Indirect Spend Categories CapEx Construction & Engineering Energy --> Inland Logistics Global Ocean & Air Freight Travel Fleet Management Consulting, Professional & Financial Services Temp Labor & Recruitment --> Human Resources Legal Services IT & Telecom Marketing Marketing – Creative & (..)

Packaging 90

Packaging 90

Putting Patients First Blog

FEBRUARY 1, 2024

Since it is likely this appropriations package will be one of the last meaningful pieces of legislation before the November elections, other policy priorities may be added to that final legislation as it gets closer to passage. We reiterated these priorities to start the year in January 2024.

Insurance Coverage and Processing 52

Insurance Coverage and Processing Packaging Hospitals 52

Express Pharma

JUNE 2, 2023

As part of these efforts, the government has implemented regulations mandating API (active pharmaceutical ingredient) manufacturers and pharma brands to incorporate barcoding on product packaging. This regulatory step is aimed at preventing falsified medicines from entering the market.

Adverse Reactions 103

Adverse Reactions Packaging Documentation Dosage 103

FDA Law Blog: Biosimilars

JULY 10, 2023

In this blog post, we will first briefly outline the procedural steps in the 510(k) review process for medical devices. However, the strategy of addressing the AI request presented in the next section of this blog post applies to all three types of 510(k)s. FDA Day (in calendar days) FDA Actions Day 1 FDA receives 510(k) submission.

Documentation 75

Documentation Packaging Communication Labelling 75

Pharma and Life Sciences Blog

JANUARY 16, 2025

Read this case study to learn how a global pharmaceutical leader fixed inefficiencies in a 25M packaging budget. How GEP Helped a Pharma Company Save $2M With Sustainable Sourcing priyanka.katke Thu, 01/16/2025 - 16:02 Balancing sustainability goals with cost efficiency in your supply chain management is no small feat.

Packaging 52

Packaging 52

Putting Patients First Blog

JULY 18, 2023

In his remarks, Reiser discussed the current dynamics on the Hill and the possibility of an end-of-year health care package. Other Blogs: The Benefits of NHC Membership 07/25/2023 Read More Why is mental health awareness foundational for diverse communities?

Packaging 52

Packaging Biosimilars 52

FDA Law Blog: Biosimilars

MARCH 8, 2023

Background FDA first introduced the final rule and guidance on eMDR in 2014 , which we blogged about here. For any major changes, additional time will be granted between the release of the implementation package and production deployment. User facilities are not required, but have been encouraged, to submit MDRs electronically.

Packaging 59

Packaging Communication 59

Pharma Marketing Network

AUGUST 9, 2023

In this blog post, we will explore best practices for pharmaceutical companies to navigate the complex landscape of regulatory challenges in marketing. Adhere to Labeling and Packaging Requirements The labeling and packaging of pharmaceutical products are tightly regulated to ensure safety and accurate information.

Labelling 52

Labelling Packaging Communication Pharmaceutical Companies 52

FDA Law Blog: Biosimilars

SEPTEMBER 24, 2024

Before FDA even asked, we had been considering an HPM FDA Law Blog post on this subject. The appeal of distilling down the extensive process that goes into the decision to approve an application into a single package is easy to see, and some may be interested in only the ultimate distillation – an approval is issued or not.

Documentation 59

Documentation Packaging 59

FDA Law Blog: Biosimilars

AUGUST 27, 2023

FDA intends the Guidance to provide “clarity and flexibility” to trading partners to “help ensure continued patient access to prescription drugs as the supply chain transitions to the interoperable, electronic product tracing at the package level under the DSCSA” while supporting “continued availability of products to patients.”

Packaging 52

Packaging 52

FDA Law Blog: Biosimilars

MARCH 21, 2024

As readers of our blog know, MoCRA was a significant change to regulation of cosmetics. Now in the second year of implementation, companies have started noticing the consequences as FDA implements the new requirements and develops regulations and guidance.

Packaging 64

Packaging Communication 64

Express Pharma

SEPTEMBER 8, 2023

What assurance is there that counterfeiters who can easily mimic a brand’s packaging, name, and logo won’t also be able to mimic its QR codes? Google lens : Utilise the powerful visual recognition capabilities of Google Lens to capture and interpret codes on the packaging swiftly. System workflow 1.

Packaging 52

Packaging Labelling 52

Putting Patients First Blog

AUGUST 2, 2023

Throughout a hearing on July 13, Energy and Commerce Democrats urged for measures to address drug shortages, however Republican leadership echoed their stance that drug shortages are irrelevant to PAHPA and should be addressed in a separate package. The NHC will continue to monitor any new developments as they arise in the coming weeks.

Packaging 52

Packaging 52

Pharmacy Joe

OCTOBER 25, 2023

ISMP encourages organizations to maintain, update, and periodically review a list of oral dosage forms that may require alteration through evaluation of package inserts, drug manufacturer inquiries, tertiary drug information resources, and primary literature.

Dosage 111

Dosage Inpatient Packaging Documentation 111

FDA Law Blog: Biosimilars

FEBRUARY 21, 2024

The long-awaited final rule, which we last discussed in a July 2023 blog post and have tracked in our March 2023 and March 2022 posts, aims to harmonize quality management system requirements for medical devices with requirements set forth by other regulatory authorities around the world. Notably, Part 820 will look different.

Labelling 59

Labelling Packaging Documentation 59

Quality Matters

NOVEMBER 5, 2024

Food and Drug Administration (FDA) by API manufacturers to provide confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of human drug products. Read USP’s paper for strategies to enable geographic diversity of the medicines supply chain. _

Pharmaceutical Manufacturing 78

Pharmaceutical Manufacturing Packaging Documentation 78

epicur

MAY 6, 2024

In her recent Meet the Team blog, Advisory Council member Nicole Clausen shared great insights on how far veterinary inventory management has come since she joined the profession. You can read that blog here! You can read that blog here! How easy is it to order from them? Are there any barriers to the ordering process?

Customer Service 52

Customer Service Compounding Chemotherapy Online Pharmacies 52

FDA Law Blog: Biosimilars

MARCH 27, 2023

Such codes need to be placed on device labels and packages to allow devices to be easily identified and tracked throughout their lifecycle, except where the rule provided for an exception or alternative. Once the device is required to bear a UDI, any NHRIC and NDC codes will no longer be permitted on the device label or device packaging.

Labelling 45

Labelling Packaging Documentation 45

The Honest Apothecary

MAY 7, 2023

Here I share some of the latest news, articles, editorials, or blog posts that fall generally under the theme of Pharma or healthcare. I might throw in a something off-topic from time to time which I found while wandering throughout the endless hallways and corridors of the internet. ” PATCH. “lēf Farms of Loudon, N.H.

Hospitals 52

Hospitals Packaging 52

National Association of Boards of Pharmacy

OCTOBER 23, 2024

Exchanging transaction information, verifying product identifiers, responding to regulator requests for transaction information, and gathering transaction information at the package level. ATPs must have a process in place for  identifying  and investigating suspect and illegitimate products.  

Packaging 49

Packaging Documentation Pharmacy Technician 49

Pharma Marketing Network

AUGUST 9, 2023

In this blog post, we will explore best practices for pharmaceutical companies to navigate the complex landscape of regulatory challenges in marketing. Adhere to Labeling and Packaging Requirements The labeling and packaging of pharmaceutical products are tightly regulated to ensure safety and accurate information.

Labelling 40

Labelling Packaging Communication Pharmaceutical Companies 40

Pharma and Life Sciences Blog

DECEMBER 12, 2023

Explore the report Executive Summary Indirect Spend Categories CapEx Construction & Engineering Energy --> Inland Logistics Global Ocean & Air Freight Travel Fleet Management Consulting, Professional & Financial Services Temp Labor & Recruitment --> Human Resources Legal Services IT & Telecom Marketing Marketing – Creative & Production --> Maintenance, (..)

Packaging 59

Packaging 59

FDA Law Blog: Biosimilars

SEPTEMBER 27, 2023

The meeting package for Type D meetings should be included with the meeting request. FDA intends to provide preliminary responses to Type D meeting packages no later than 5 calendar days before the meeting date. The goal for meeting minutes is the same as all other meeting types – 30 days after the meeting.

Packaging 64

Packaging Drug Development Documentation 64

Pharma and Life Sciences Blog

JUNE 23, 2023

A new case study from GEP details how a global consumer packaged goods manufacturer transformed its source-to-pay processes to improve focus on indirect spend and deliver significant savings.

Packaging 52

Packaging 52

Express Pharma

JUNE 28, 2023

Other related technologies such as scanning barcode labels on packages have also facilitated electronic purchasing and procurement on a larger scale. However, a management system can help ensure the security and availability of all medicine stocks, resulting in cost savings.

Online Pharmacies 98

Online Pharmacies Customer Service Data Entry Packaging 98

Express Pharma

APRIL 6, 2023

To achieve this, startups should implement rigorous quality control measures throughout their production processes, from sourcing ingredients to manufacturing and packaging. In addition to implementing quality control measures, startups must also comply with labelling and advertising regulations.

Labelling 98

Labelling Dosage Packaging Documentation 98