Medical device regulatory affairs operational transformation
Key insights and opportunities to unlock additional value by streamlining Regulatory Affairs operational activities
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Opportunities in an evolving market
2019 Health Care & Life Sciences Investment Outlook
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Pathways to Success
Medicare Shared Savings Program
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Promoting interoperability
CMS and ONC proposed rules on the exchange of health information
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Quality 2030
Forward-thinking Life Sciences CXOs will transform Quality from a cost center to a value creator
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The Race to EU MDR Compliance Continues - Full Results
Despite progress over the past year, medical device companies are still facing many questions, according to annual KPMG/RAPS survey.
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The Race to EU MDR Compliance Continues
Despite progress, companies are still facing many questions
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The clinical trial conundrum
Failing to resume clinical trials could present as many risks to certain patients as COVID-19
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Generics 2030: Three strategies to curb the downward spiral
By 2030, generics manufacturers will need to shift from the status quo and explore one of three avenues for change.
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Re-launching elective procedures
An opportunity for medical device companies to shape their future customer base
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Episode 3: Physician compensation
This podcast explores how compensation trends are evolving with physician practices and what implications recent legislative changes have had on physician compensation.
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CARES Act Provider Relief Fund Evaluation and Management
Before accepting funding under the CARES Act, providers should become familiar with the terms and conditions, know the risks, and develop plans to manage the funds.
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Cash Generators for Healthcare Organizations: Federal Edition
We will discuss opportunities for healthcare organizations to generate cash using federal income tax strategies.
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Cash Generators for Healthcare Organizations: SALT Edition
We will discuss opportunities for healthcare organizations to generate cash using both direct and indirect state and local tax solutions.
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The Clock is Reset…Opportunity for your Organization to Re-Evaluate compliance to EU MDR Labeling
A Webinar from the Specialists at KPMG & PRISYM ID on Meeting the Updated Timelines for EU MDR Labeling
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