European Pharmaceutical Review

OCTOBER 21, 2022

NCIMB Ltd provides microbial identification services and curates The National Collection of Industrial, Food and Marine Bacteria – one of the culture collections that makes up the UK Biological Resource Centre Network.

Pharmaceutical Manufacturing 85

Pharmaceutical Manufacturing 85

pharmaphorum

MAY 18, 2022

The benefits of conducting a regular KOL validation exercise to refresh your KOL list are well established. KOL validation should therefore be treated in opportunity to go well beyond just refreshing your list of KOLs. Services & Innovations Associate Executive. SIDDIQAH KHANOM. e: siddiqah.khanom@systemanalytic.com.

52

52

pharmacy mentor

APRIL 26, 2023

In this article, we explore 6 ways ChatGPT can integrate into pharmacy practice, streamlining processes, enhancing customer service, and optimising operations. Additionally, ChatGPT can assist in automatically validating prescriptions, identifying potential errors, and ensuring compliance with legal and regulatory requirements.

Customer Service 52

Customer Service Process Improvement Communication 52

European Pharmaceutical Review

MARCH 5, 2024

Visitors can gain insights into compliance with industry-specific validation guidelines and requirements such as GMP , GLP, REACH and FDA. The search for sustainable alternatives also extends to chemicals and laboratory utensils, while the trend toward miniaturisation helps conserve resources and reduce waste.

Labelling 94

Labelling 94

Drug Channels

SEPTEMBER 12, 2023

9 chapters, 300+ pages, 163 exhibits, 600+ endnotes: There is nothing else available that comes close to this valuable resource. Special preorder and launch pricing discounts will be valid through October 20, 2023. pharmaceutical distribution industry. This means that you can be among the first to access our new report.

Biosimilars 52

Biosimilars 52

Integra X Files

MAY 22, 2023

There are circumstances where PA is entirely appropriate, especially when it comes to the use of low-value healthcare services. When PA is used to raise the bar for access to low-value healthcare services, there should be a benefit to individual patients and savings to the system.

Insurance Coverage and Processing 94

Insurance Coverage and Processing Health Insurance Companies 94

pharmaphorum

NOVEMBER 20, 2022

Early engagement with a specialised partner can be critical: the partner will have resources and ready-to-go solutions to act as an extension of a sponsor’s laboratories, keeping pace with quick timelines without compromise. Using in-house assay catalogues saves on development and validation time and can help accelerate a vaccine programme.

Vaccines 98

Vaccines Immunity Immunization 98

Syner-G

SEPTEMBER 20, 2023

Results Syner-G provided services as an extended QA team for the client. Solution Syner-G provided the QA resource (Person-in-Plant) to review and approve DS and DP in early phase development and Phase III clinical. QA resource must ensure phase appropriate GMP compliance and QMS activities related to the project have to be tracked.

Documentation 40

Documentation Communication 40

pharmaphorum

SEPTEMBER 24, 2020

In summary, they must: Continue to accelerate the return to normal levels for non-COVID health services. This is a huge ask on already stretched services. Without appropriate action now to manage patient data, the corrective recovery could take an enormous amount of time and resources”. Prepare for winter pressures.

Data Entry 111

Data Entry Documentation Hospitals 111

Drug Channels

SEPTEMBER 21, 2020

This important event convenes key stakeholders including manufacturers, specialty pharmacies, hubs, payers, PBMs, physicians and more to explore strategies for developing and integrating hub programs and other patient-centric services to ensure product access and optimal reimbursement. Arquette, R.Ph., REGISTER TODAY.

Specialty Pharmacies 52

Specialty Pharmacies 52

Pharmaceutical Technology

AUGUST 10, 2022

Companies may look at one service today, but will likely expand their scope in the future, so it’s important that the provider can evolve with a given project.??. While a potential service provider’s capabilities and track record should be well understood, companies shouldn’t choose a CMO based just on cost. Process Flow diagram?

Packaging 52

Packaging Communication 52

pharmaphorum

JULY 18, 2022

This means even more associated costs, resources, time, and effort. Formedix lets you build, preview, and validate studies for most EDC systems. That’s the kind of time and resource-saving you’re looking at. The time and resources you save mean potential cost savings too. As you know, clinical trials can be complex.

Communication 98

Communication 98

Express Pharma

APRIL 2, 2024

For example, drug repurposing can use data mining and network analysis to identify new indications for approved or failed drugs, thus saving time and resources. Drug development These new-age technologies can improve the drug development process by enabling faster and more reliable validation, optimisation and scale-up of drug candidates.

Drug Development 59

Drug Development Clinic Management Communication 59

pharmaphorum

NOVEMBER 9, 2020

Managed by Medicines Discovery Catapult, the Psychiatry Consortium comprises prominent players across industry, charities and academia, working together to develop and deliver a portfolio of innovative and collaborative projects, which focus on identifying and validating new therapeutic targets for psychiatric diseases.

52

52

pharmaphorum

AUGUST 4, 2021

Standardizing metadata reduces the resources, effort, and time spent setting up studies. Validation. Every clinical MDR should have validation built in every step of the way. Validation and reporting highlight any compliance deviations from regulatory standards, and alert users as to where issues reside. The result?

Communication 98

Communication Documentation 98

GMPSOP

JULY 23, 2023

If you remember the (V) shaped model that is commonly used to map the computer system validation life cycle? If you are completely unfamiliar with what is installation qualification then we suggest you read the article Validation in Pharmaceutical Industry first. If there is a Validation Protocol provide a reference of the protocol no.

Documentation 52

Documentation Method Validation Packaging Labelling 52

pharmaphorum

JULY 8, 2022

Preliminary research suggests that hybrid DCTs can reduce trial timing and resources , improve patient-centricity and patient engagement , and expand access and recruitment and increase diversity , mitigate bias, and reinforce inclusion in clinical trials.

Drug Development 100

Drug Development Diabetes 100

Syner-G

AUGUST 9, 2022

The software was validated to ensure 21 CFR Part 11 compliance and the associated standard operating procedures were finalized. By early 2014, the Regulatory Operations group was fully operational and ready to offer electronic publishing services to IMPACT’s clients. The staff to manage and support this group was secured.

Packaging 40

Packaging Documentation 40

Digital Pharmacist

NOVEMBER 23, 2022

Section 179 is valid on most types of equipment. To qualify for a Section 179 deduction, the equipment must have been purchased (or leased/financed) and placed into service by midnight, December 31st of the year you are taking the deduction for. Digital Pharmacist Marketing Services. How can Section 179 affect your pharmacy?

Pharmacy Automation 52

Pharmacy Automation Communication Pharmacy Management 52

FDA Law Blog: Biosimilars

NOVEMBER 2, 2023

We are also aware that FDA spends a tremendous amount of time and resources answering the same questions for sponsors. Voluntary consensus standards will not design the measuring tools, but they will help companies validate these tools and define acceptable results.

Packaging 59

Packaging Documentation Labelling Communication 59

pharmaphorum

NOVEMBER 4, 2021

This means even more associated costs, resources, time, and effort. Formedix lets you build, preview, and validate studies for most EDC systems. That’s the kind of time and resource-saving you’re looking at. The time and resources you save mean potential cost savings too. As you know, clinical trials can be complex.

Communication 52

Communication 52

European Pharmaceutical Review

JUNE 29, 2023

To amplify and ease the implementation of guidance from global regulators, USP responded with a suite of innovative standards, services and solutions. In response, USP developed educational resources to support manufacturers and scientists on analytical procedures such as mass spectrometry for monitoring nitrosamine impurities.

Compounding 94

Compounding 94

GMPSOP

MAY 26, 2023

Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: June 3, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.

Documentation 52

Documentation Packaging Communication Customer Service 52

GMPSOP

MAY 26, 2023

Six steps process to implement change control management Pharmaceuticals quality assurance & validation procedures GMPSOP Six steps process to implement change control management Last modified: May 28, 2023 Table of Contents “It is not the strongest of the species that survive, nor the most intelligent, but the one most responsive to change”.

Documentation 52

Documentation Packaging Communication Customer Service 52

pharmaphorum

DECEMBER 29, 2022

At the same time, the industry must address the long-term difficulty of providing essential medicines and health services to the high percentage of global population that cannot access them because of costs. Fast implementation of new processes through modelling and simulation. Staying one step ahead of unplanned downtime and disruption.

Vaccines 111

Vaccines 111

Quality Matters

JUNE 6, 2023

Using a risk-based approach to quality, tools and resources can be allocated more efficiently, and high-risk excipients can be more rigorously evaluated to safeguard the quality of the final drug product. The risks associated with excipients also should be considered based on specific manufacturing operations and product formulations.

Dosage 52

Dosage Packaging Documentation Drug Development 52

pharmaphorum

JANUARY 18, 2021

We’ve seen extreme seasonal cycles of weather for several years now, which has upped demand for all services like ambulance, A&E and mental health care. Services used, in some regard, by pretty much every societal section. There are many factors at play driving this. Dealing in data quality. Capitalising on the rest opportunity.

Compounding 95

Compounding Hospitals 95

pharmaphorum

JULY 28, 2022

In a time of uncertainty, companies must ensure that their systems function as intended, have enough resources, and follow the correct procedures. With on-site FDA inspections starting again, it’s imperative that businesses reassess their processes and workforce now to remain compliant. In addition to her FDA experience, Ms.

Diabetes 111

Diabetes Dosage Pharmaceutical Manufacturing Documentation 111

pharmaphorum

MARCH 4, 2021

Rahman notes, for example, that during the COVID-19 pandemic, models created in one specific environment or country are often used to create policy in another country (often due to lack of resources) without consideration for how populations might provide different data. About Intouch Group.

Compounding 106

Compounding Communication Hospitals Drug Development 106

PharmaState Academy

MARCH 4, 2024

This methodology typically includes: Internal Assessment: Gathering data on company resources, capabilities, and performance metrics to identify strengths and weaknesses. This may involve triangulating findings from multiple data sources and validating conclusions through peer review and stakeholder feedback.

Pharmaceutical Companies 52

Pharmaceutical Companies Pharmaceutical Companies 52

PharmaState Academy

MARCH 3, 2024

This methodology typically includes: Internal Assessment: Gathering data on company resources, capabilities, and performance metrics to identify strengths and weaknesses. This may involve triangulating findings from multiple data sources and validating conclusions through peer review and stakeholder feedback.

Pharmaceutical Companies 52

Pharmaceutical Companies Pharmaceutical Companies 52

Viseven

JANUARY 9, 2023

Recognize and validate the sentiments of your patient out loud. of patients used telemedicine services. Department of Health and Human Services has developed the National Culturally and Linguistically Appropriate Services Standards ( CLAS ) to advance health equity, enhance quality, and assist in eliminating health care disparities.

Communication 52

Communication Hospitals Clinic Management Diabetes 52

pharmaphorum

SEPTEMBER 14, 2022

and shifted outreach resources to better reach target patients, including traditionally underserved populations, and ensure their interests and concerns were addressed. Data analytics tools also helped with monitoring recruitment success across demographics. Sponsors adapted strategies in real-time to update messaging (e.g.,

Vaccines 98

Vaccines Medical Records Documentation Communication 98

pharmaphorum

JANUARY 31, 2023

This ultimately impacts patient perception of healthcare services in general. As patients experience first-hand the effectiveness reported in clinical trials, trust in the validity of these trials and the intentions of the pharmaceutical companies that fund them improves.

Pharmaceutical Companies 52

Pharmaceutical Companies Pharmaceutical Companies Vaccines Communication 52

pharmaphorum

MAY 14, 2021

“For example, its 2013 guide to the methods of technology appraisal is still a valid reference to understand the key principles of cost effectiveness within an HTA context, and NICE decision support unit documents are a useful resource for any health economist needing technical or educational support.

Drug Pricing 59

Drug Pricing Documentation Pharmaceutical Companies Pharmaceutical Companies 59

FADIC

JULY 10, 2023

Tavus Tavus AI is a powerful tool that leverages the power of artificial intelligence to automate and optimise customer service operations. The platform’s intelligent features include natural language processing, sentiment analysis, and intelligent routing, ensuring customers relate to the right agent or resource for their needs.

Communication 52

Communication Data Entry Customer Service Documentation 52

FDA Law Blog: Biosimilars

APRIL 30, 2023

Litigation risk tilts the balance: In our experience, the prospect of taking FDA to court when it makes a mistake, violates the law, or otherwise compromises the public interest is the only tool that reliably ensures FDA will prioritize a given issue and dedicate the resources and personnel needed to resolve it quickly and appropriately.

Immunity 59

Immunity Immunization Biosimilars Labelling 59