Pharmaceutical Technology

JULY 15, 2025

The net payment made by Sino to acquire LaNova will be approximately $500.9m, a figure that excludes the estimated cash and bank deposits, according to a company document outlining the terms of the transaction. At the time, Sino spent 142 million yuan ($19.80m) to initiate its ownership involvement with the biotech.

Packaging

Pharmaceutical Technology

JULY 18, 2025

Comstock said it is not yet clear if the report will be turned into an official agency guidance document, but it will be made publicly available. Give your business an edge with our leading industry insights. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

FDA

Pharmaceutical Technology

JULY 18, 2025

The concern of ocular toxicity was first highlighted in a document published ahead of the ODAC meeting that took place on 17 July. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address. Sign up for our daily news round-up!

FDA

pharmaphorum

JULY 7, 2025

Skip to main content Monday 7 July 2025 BlueSky linkedin youtube rss User account menu Subscribe Channels Channels Digital Market Access Oncology Patients R&D Sales & Marketing Spotlight on Content type Content type Digital -News -Views & Analysis -Deep Dive -Webinars -Podcasts -Video -White Papers -Event Market Access -News -Views & (..)

Pharmaceutical Companies

pharmaphorum

JANUARY 26, 2023

Guidance on the way pharma companies communicate about prescription medicines has been updated in the UK to cover use of social media channels for the first time. ” To help communicate the new guidance, the PMCPA is planning to run two webinars next month for companies and media organisations, on 9 February and 21 February.

Communication

pharmaphorum

OCTOBER 27, 2022

The overarching principle set out in Codes of Practice, and in particular the Principles for the use of digital channels in the EFPIA Code , is that the legislation and Codes of Practice apply equally to communications by companies on social media and digital channels.

Communication

pharmaphorum

NOVEMBER 15, 2021

That was among the key messages from speakers at a joint European Forum for Good Clinical Practice (EFGCP) and the European Federation of Pharmaceutical Industries and Associations (EFPIA) webinar, held last week. This should cover the entire process, “starting with the writing, the review of the document, and its dissemination”.

Documentation

PQA

DECEMBER 1, 2023

In support of this goal, PQA has performed a review of its bylaws and proposes revisions which modernize and streamline this important governing document. If community pharmacists can easily collect these data, they can be an effective resource to promote clinical trial diversity. This webinar is supported by PQS.

Community Pharmacies

PQA

SEPTEMBER 30, 2024

Today, we published the 2024 PQA Annual Report, which documents our progress towards our strategic goals. PQA Quality Forum Webinar, on October 10, from 1-2 p.m. Members-Only Quality Forum Webinar, on November 21, sponsored by PQS by Innovaccer. 2024 PQA Leadership Summit, November 7-8 in Arlington, Va.

Specialty Pharmacies

The FDA Law Blog

FEBRUARY 27, 2023

Helpful practitioner prescribing guidance is set forth in a simplified document here. We will release exciting details of our upcoming webinar addressing telemedicine soon. Stay tuned.

Controlled Substances

Pharmaceutical Technology

DECEMBER 15, 2022

In addition, several pieces of documentation will be required to support the API qualification, e.g. pharmacopeial compliance. It is also essential to evaluate the reliability of the company supplying the ingredient: do they provide sufficient communication and documentation? It has proved to be most effective at high pH.

Documentation

PQA

MARCH 8, 2024

Offering Resources to Implement Point-of-Care Testing The National Community Pharmacists Association and National Alliance of State Pharmacy Associations have developed a new guidance document to help community pharmacy teams with their point-of-care testing services. "A prior to the PQA Leadership Summit.

Community Pharmacies

ISPE

JULY 19, 2023

and management communication strategy. In the years leading up to 2022, numerous publications were issued; networking events, webinars, and conferences were held; and regulatory panel discussions with regulators performed. Is the vendors’ documentation complete in order to assess GxP risks and GxP compliance?

Documentation

PQA

JUNE 27, 2024

This feedback was gathered via surveys and then further discussed by pilot participants during three collaborative webinars. For example, one participant described how varying levels of “urgency” could be communicated to pharmacists, empowering them to prioritize prescriptions for expedited review. Want to Learn More?

Specialty Pharmacies

The FDA Law Blog

OCTOBER 10, 2023

By Philip Won & Véronique Li, Senior Medical Device Regulation Expert — As we recently blogged , FDA released three draft guidance documents to help enhance the predictability, consistency, and transparency of the 510(k) program. One of these documents focuses on “ Evidentiary Expectations for 510(k) Implant Devices.”

Documentation

DiversifyRx

JULY 11, 2024

Join our next Awesome Webinar Series with guest legal guru JD from Real Value Rx to answer any questions you have about the DSCSA delay. To be authorized: Pharmacies should ensure they receive, maintain, and update these documents as necessary to continue ordering from their ATP and be ready to provide copies of them upon request.

Independent Pharmacies

Viseven

SEPTEMBER 13, 2024

For example, going “paperless” and moving all of the documentation to the cloud and keeping only electronic documents from now on can be considered a part of digital transformation. Communication platforms (e.g., This often means switching from usual solutions to new, more advanced ones. Digital Content Factory ).

Documentation

pharmaphorum

FEBRUARY 11, 2021

In a recent webinar from pharmaphorum, the National Institute for Health Research (NIHR) outlined why and how it has developed a new approach to engage with patients while complying with national regulations, such as those set out in the Association of the British Pharmaceutical Industry’s (ABPI) Code of Practice.

Communication

ISPE

AUGUST 29, 2022

For changes requiring approval before implementation, once the necessary information has been submitted across regions, each health authority must review the data package and documentation based on local requirements. laboratory notebooks, batch records, and technical reports) to submission documents (e.g., Accessed 7 September 2021.

Documentation

IDStewardship

APRIL 13, 2023

An important accompanying document for Joint Commission standards are Critical Access Hospital Accreditation Survey Activity Guide, for which the January 2023 guide can be found here. The latest antimicrobial stewardship regulations from The Joint Commission went into effect in January 2023.

Hospitals

Viseven

JULY 12, 2022

There are three main types of medical website content resources you can use for that: Webinars. Healthcare marketing apps can help marketers optimize their daily activities such as task organization, team communication, customer engagement, results tracking, and beyond. Master Modular Content Creation.

Communication

DiversifyRx

JULY 15, 2024

Whether it’s a new marketing technique, an efficient workflow process, or tips on managing inventory, sharing these with your peers can elevate the entire community. Encourage Open Communication: Create platforms where pharmacy owners can discuss challenges and share solutions. A great place to learn is our BLOG.

Independent Pharmacies

The FDA Law Blog

FEBRUARY 5, 2025

Lenz, Principal Medical Device Regulation Expert In early January, FDA released a draft guidance document titled Artificial Intelligence-Enabled Device Software Functions: Lifecycle Management and Marketing Submission Recommendations (Draft AI Guidance). By Adrienne R. User Interface Software Description Section VI.B

Documentation