Bio Pharma Dive

AUGUST 9, 2021

Receive drug conversion and submission services by our expert staff, to remain compliant with the FDA.

Compliance 246

Compliance Drugs 246

Drug Patent Watch

MARCH 26, 2025

In our latest blog post, we delve into the compliance hurdles that generic drug developers face, and the valuable lessons learned from these experiences. This not only helps to ensure compliance, but also fosters a culture of trust and cooperation within the industry. Share your experiences with us in the comments below!

Generic Drugs 52

Generic Drugs Compliance Development Drugs 52

ACRP blog

FEBRUARY 11, 2025

The Health Care Compliance Association (HCCA), a nonprofit membership organization supporting healthcare compliance professionals, was founded, in part, to be your eyes and ears for compliance updates and regulatory changes. Group discounts are available; bring your team for shared learning!

Compliance 59

Compliance Clinical Research Research Regulation 59

Pharmaceutical Technology

APRIL 19, 2024

Pharmaceutical Compliance Management Software Is Designed to Enhance Patient Safety. Download the Free Buyer’s Guide Here.

Compliance 130

Compliance 130

World of DTC Marketing

SEPTEMBER 12, 2022

There are many reasons for non-compliance and non-adherence: Cost and affordability, lack of understanding/comprehension of advice, language barriers, cognitive abilities, fear of asking for clarification, or other reasons. The post Is Apple that naive when it comes to compliance? Oh, to live in an ideal world.

Compliance 166

Compliance Doctors Doctor Production 166

ACRP blog

JANUARY 28, 2025

However, if the personal data relates to European Union (EU) or United Kingdom (UK) residents, this raises particular legal and compliance issues due to the General Data Protection Regulation (GDPR). Edited by Jill Dawson The post Research, Innovation, and Compliance in the EU and UK: A Data Privacy Roadmap appeared first on ACRP.

Compliance 59

Compliance Research Clinical Trials Clinical Trials 59

Bio Pharma Dive

SEPTEMBER 16, 2024

NGS is changing the landscape for GxP compliance. How can you adapt?

Compliance 130

Compliance 130

Pharma Mirror

NOVEMBER 7, 2023

Navigating regulatory compliance in the pharmaceutical industry is crucial to ensure the safety, efficacy, and quality of pharmaceutical products. Good Manufacturing Practices The post Navigating Regulatory Compliance in the Pharmaceutical Industry appeared first on Pharma Mirror Magazine.

Compliance 130

Compliance Regulation Manufacturing Production 130

Pharmaceutical Technology

MARCH 26, 2024

KOLs interviewed by GlobalData emphasised urgent action to address inconsistent drug compliance rates in the osteoporosis disease landscape.

Compliance 130

Compliance Drugs 130

Pharmaceutical Technology

AUGUST 22, 2023

Qualifyze has secured $12m to improve supply chain compliance in the pharmaceutical sector using technological and audit data.

Compliance 130

Compliance 130

Pharmaceutical Technology

JULY 15, 2024

AstraZeneca has obtained Health Canada’s Notice of Compliance (NOC) for Tagrisso (osimertinib) to treat NSCLC.

Compliance 287

Compliance 287

pharmaphorum

DECEMBER 23, 2024

Stay updated on the latest Good Manufacturing Practices (GMP) and quality compliance standards in the digital era with our comprehensive guide. Learn how to ensure your products meet regulatory requirements.

Compliance 105

Compliance Manufacturing Production 105

pharmaphorum

JULY 17, 2024

Discover how artificial intelligence is revolutionising drug development and compliance in the pharmaceutical industry with these four impactful ways.

Compliance 111

Compliance Development Drugs 111

pharmaphorum

JANUARY 22, 2024

Pharma waste management is crucial for balancing cost, compliance, and environmental responsibility in the healthcare industry. Explore strategies and best practices for effectively managing pharmaceutical waste, while ensuring regulatory compliance and minimising environmental impact.

Compliance 113

Compliance 113

pharmaphorum

OCTOBER 1, 2024

Learn how Advanced Clinical ensures compliance through the Functional Point of Contact (FPOC) story. Explore their innovative approach to maintaining regulatory standards.

Compliance 105

Compliance 105

Pharma Marketing Network

MARCH 6, 2025

This article explores effective social media advertising strategies tailored for pharmaceutical marketing executives , helping them navigate compliance and create impactful campaigns. Ensuring Compliance in Pharma Social Media Ads Navigating regulatory compliance in pharma social media advertising is one of the biggest challenges.

Compliance 52

Compliance Branding Marketing Regulation 52

pharmaphorum

APRIL 30, 2024

Discover strategies for enhancing compliance and resilience in pharmaceutical supply chains through effective monitoring, due diligence, and understanding the impact on the industry. Find out more.

Compliance 101

Compliance 101

Cloudbyz

AUGUST 30, 2024

Given the critical nature of this data, ensuring its security and compliance with regulatory standards is paramount. Regulatory Penalties: Non-compliance with data protection regulations can lead to hefty fines and legal actions. Here are key strategies to ensure compliance within CTMS.

Compliance 97

Compliance Clinical Trials Clinical Trials Trials 97

Cloudbyz

AUGUST 30, 2024

The introduction of Clinical Trial Management Systems (CTMS) has revolutionized how trials are conducted by streamlining operations, enhancing regulatory compliance, and reducing the risk of errors. Managing these trials efficiently while ensuring compliance with stringent regulatory standards is paramount to their success.

Compliance 93

Compliance Clinical Trials Clinical Trials Trials 93

Pharmaceutical Technology

NOVEMBER 22, 2024

Health Canada has issued a Notice of Compliance (NOC) for Johnson & Johnson’s (J&J) CARVYKTI for multiple myeloma treatment.

Compliance 246

Compliance 246

Pharmaceutical Technology

OCTOBER 17, 2023

As AI applications in drug manufacturing widen, Leucine’s digital twin of the shop floor helps automate compliance and improve safety.

Manufacturing 264

Manufacturing Compliance Drugs 264

Pharmaceutical Technology

OCTOBER 20, 2023

Health Canada has granted a Notice of Compliance (NOC) to Sumitomo Pharma Canada and Pfizer Canada’s MYFEMBREE.

Compliance 246

Compliance 246

Bio Pharma Dive

JULY 3, 2023

iliomad Health Data can help you maintain GDPR compliance. What is the GDPR and why does it matter to your life sciences company.

Life Science 246

Life Science Compliance Trials 246

Pharmaceutical Technology

OCTOBER 28, 2024

Ahead of the upcoming DSCSA November deadline, pharma companies reimagine track-and-trace to tackle the US counterfeit drug landscape.

Compliance 130

Compliance Pharma Companies Drugs 130

Drug Patent Watch

DECEMBER 10, 2024

Here, we will explore how CDMOs can provide support in regulatory compliance, ensuring that products meet the strict demands of safety, purity, and efficacy. Risk Mitigation CDMOs help mitigate risks associated with regulatory compliance by ensuring that products meet the required standards. Societal CDMO. link] UPM Pharmaceuticals.

Compliance 98

Compliance Manufacturing Production Regulation 98

Pharmaceutical Technology

OCTOBER 10, 2024

At CPHI Europe, an expert discussed the promise of gummies as a drug delivery system and their unique manufacturing challenges.

Drug Delivery Systems 130

Drug Delivery Systems Drug Delivery Compliance Drugs 130

Pharmaceutical Technology

MARCH 6, 2025

Post-authorisation safety studies (PASS) are often seen simply as a regulatory necessity, a checkbox that ensures ongoing monitoring of a treatments safety. However, for biotech and pharma focused on developing rare disease therapies, PASS can be so much more.

Compliance 130

Compliance Development 130

Pharma Marketing Network

FEBRUARY 19, 2025

This guide explores the best strategies for boosting engagement while ensuring compliance , helping pharma brands connect with their audiences more effectively. Regulatory-Friendly Communication : Unlike social media ads, emails offer controlled messaging that aligns with compliance regulations.

Compliance 72

Compliance Marketing Branding Regulation 72

Cloudbyz

SEPTEMBER 12, 2024

In clinical trials, ensuring data quality is crucial for both the success of the trial and regulatory compliance. By discussing sophisticated use cases and best practices, we offer an in-depth perspective on how to implement effective edit checks for maximal data accuracy, compliance, and efficiency. Core Types of Edit Checks 1.

Compliance 96

Compliance Clinical Trials Clinical Trials Trials 96

AuroBlog - Aurous Healthcare Clinical Trials blog

MARCH 18, 2024

In a move aimed at enhancing compliance and facilitating smoother trade operations, the Directorate General of Foreign Trade (DGFT) has introduced stringent policy conditions for the export of chitin and chitosan derivatives.

Regulation 184

Regulation Compliance Marketing Clinical Trials 184

Pharmaceutical Technology

NOVEMBER 8, 2023

With an era of digital transformation promising to optimise pharmaceutical supply chains, how are companies learning to embrace the change?

Compliance 130

Compliance 130

Drug Patent Watch

DECEMBER 11, 2024

As the world grapples with the consequences of climate change, companies must adapt their operations to reduce environmental impacts while maintaining cost-effectiveness and regulatory compliance. Regulatory Compliance and Incentives Regulatory compliance is a critical aspect of sustainable generic drug development.

Generic Drugs 98

Generic Drugs Development Drugs Compliance 98

Drug Patent Watch

JANUARY 29, 2025

Factors such as raw material sourcing, manufacturing costs, regulatory compliance, and distribution networks all contribute to the final price of the generic medication. Regulatory compliance is another significant factor influencing the affordability of generic medications. Sounds straightforward, right?

Generic Drugs 78

Generic Drugs Production Compliance Drugs 78

Worldwide Clinical Trials

JUNE 13, 2024

The study focused on several key factors: DNA Yield and Quality Sample Stability Assay Outcomes Patient Compliance DNA Yield and Quality The study found that blood samples typically yield a higher quantity of DNA compared to buccal swabs. Buccal swabs had a compliance rate of 95%, compared to 69% for blood samples.

Medicine 182

Medicine DNA Compliance Clinical Trials 182

AuroBlog - Aurous Healthcare Clinical Trials blog

SEPTEMBER 12, 2024

In a significant move to enhance trade facilitation and streamline compliance with foreign trade regulations, the Directorate General of Foreign Trade (DGFT), under the Ministry of Commerce & Industry, has announced amendments to the export obligation period for several import items.

Compliance 188

Compliance Regulation Drugs Clinical Trials 188

Pharmaceutical Commerce

SEPTEMBER 3, 2024

In an interview with Pharma Commerce Editor Nicholas Saraceno, Ilisa B.G. Bernstein, President of Bernstein Rx Solutions, LLC, highlights the hard-hitting points that she anticipated will be covered during her session at the 2024 HDA Traceability Seminar.

Compliance 105

Compliance 105

XTalks

DECEMBER 9, 2024

The draft also formalizes withdrawal procedures for non-compliance, including delayed studies or failure to confirm benefits. Notably, the FDA can now mandate that confirmatory trials begin before approval, ensuring proactive validation of clinical benefits.

Clinical Trials 105

Clinical Trials Clinical Trials Compliance Trials 105