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 101

Communication Documentation Hospitals Vaccines 101

PQA

MARCH 3, 2023

The PQA Quality Forum Webinar is a regular, recurring series on healthcare quality topics with a focus on medication use and medication services. The second edition of the guide documents real-world SDOH services that are promising for improving the quality and safety of medication use.

Vaccines 52

Vaccines Documentation Community Pharmacies 52

PQA

JULY 28, 2023

On the technology end, apps, videos, social media, webinars, websites and other tools reach patients wherever they are. Save the date for the next Quality Essentials Webinar on September 20, 1:00-2:00 pm ET. Initiatives include informational leaflets to one-on-one sessions with specially trained pharmacists and dietitians.

Documentation 40

Documentation Vaccines 40

PQA

AUGUST 8, 2022

In the October 2021 edition of the American Journal for Managed Care, EQUIPP® was highlighted in an article on how a collaborative effort of MAPD plans with community pharmacies could impact vaccination rates for pneumonia and influenza by providing low site of care cost immunizations to the populations served. Sheer et al., McCullough, J.,

Independent Pharmacies 52

Independent Pharmacies Community Pharmacies Patient Care Vaccines 52

PQA

JUNE 16, 2023

Additional medical services beyond vaccinations are becoming more routine at pharmacies. Your Next Engagement Opportunities Network, Learn and Collaborate with PQA Save the date for the next PQA Quality Forum Webinar, July 20, 1-2 pm ET. data sources), and usability.

Documentation 40

Documentation Vaccines 40

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 52

Documentation FDA Communication Packaging 52