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EVENTS

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Pharmacoepidemiology & Therapeutic Risk Management
PHARMACOEPIDEMIOLOGY & THERAPEUTIC RISK MANAGEMENT
August 26-30, 2020
36th International Conference on Pharmacoepidemiology & Therapeutic Risk Management (ICPE) is organized by International Society for Pharmacoepidemiology (ISPE) and will be held from Aug 26 - 30, 2020 at Estrel Berlin, Berlin, Germany.

Update CME - Internal Medicine & Primary Care
UPDATE CME - INTERNAL MEDICINE & PRIMARY CARE
October 29-01, 2020
Earn 30 CME Credits by attending our Update CME Internal Medicine and Primary Care Conference either in person or via live stream!Expert speakers from The University of Chicago, Johns Hopkins, and University of California, Los Angeles will be presenting on the latest clinical guidelines. We offer in...

Vital Signs EMS Conference
VITAL SIGNS EMS CONFERENCE
October 29-01, 2020
Vital Signs EMS Conference will be showcasing many of the extraordinary aspects of EMS and healthcare found only in Saratoga Springs. This event provided high quality and cutting edge EMS education by providing access to national and world-renowned educators through a forum that is accessible and af...

Symposium on Advanced Wound Care Fall
SYMPOSIUM ON ADVANCED WOUND CARE FALL
October 30-01, 2020
The Symposium on Advanced Wound Care Fall meeting (SAWC Fall) serves as a forum to connect the entire wound care team — physicians, nurses, physical therapists, researchers, scientists, podiatrists, and dietitians — with the foremost experts in wound care to improve patient outcomes thro...

Internal Medicine for Primary Care
INTERNAL MEDICINE FOR PRIMARY CARE
October 30-01, 2020
The Internal Medicine for Primary Care conference will cover areas like Internal Medicine for Primary Care Physicians, Issues in Women's Health Cardio, Pulmonary for Primary Care Physicians, Neurology for the Non-Neurologist.

Virginia Clinical Research Conference
VIRGINIA CLINICAL RESEARCH CONFERENCE
November 02-02, 2020
Virginia Clinical Research Conference is a one-day event that brings research teams from across Virginia together to collaborate and strengthen the statewide clinical research enterprise.

Annual Pharmaceutical and Medical Device Compliance Congress
ANNUAL PHARMACEUTICAL AND MEDICAL DEVICE COMPLIANCE CONGRESS
November 04-06, 2020
The Pharmaceutical and Medical Device Compliance Congress will gather senior compliance professionals and legal counsel from the largest research-based pharmaceutical manufacturers and aims to promote effective corporate compliance programs.

Canna-Pharma
CANNA-PHARMA
November 05-06, 2020
Canna-Pharma will explicitly link current knowledge and practice in the pharmaceutical and cannabis industries, providing a forum for scientific dialogue aimed at both advancing and applying best practices in this growing field. Research scientists, analytical experts, drug developers, drug-device m...

Pharmaceutical Meeting Professionals Summit
PHARMACEUTICAL MEETING PROFESSIONALS SUMMIT
November 05-06, 2020
Pharmaceutical Meeting Professionals Summit brings together conference and event planners from pharma, biotech, and medical device companies to discover new technology and event services while networking and building mutually beneficial relationships with third-party planners, vendors, and venue adm...

American Pharma Outsourcing Summit
AMERICAN PHARMA OUTSOURCING SUMMIT
November 05-06, 2020
Designed to provide pharmacy outsourcing executives with current trends, strategic insights and best practices in manufacturing, outsourcing, capacity management, Quality Assurance, Quality Control, regulatory compliance, Operational Excellence, supply chain and logistics. Network with over 150 of y...

Pharmacovigilance
PHARMACOVIGILANCE
December 01-03, 2020
Pharmacovigilance will bring together top pharmaceutical, biotechnology and regulatory representatives under one roof that will address the key issues of the industry. The entire program will cover the detection, analysis and prevention of adverse drug reactions. It will be studied with the help of ...

Controlled & Modified Drug Release Summit
CONTROLLED & MODIFIED DRUG RELEASE SUMMIT
December 01-03, 2020
By attending the unique Controlled & Modified Drug Release Summit, you will learn directly from 50+ of industry’s leading experts and hear multiple unique case study sessions and take-home examples to enhance your product pipeline. Gather insights into the latest technologies ...

Peptide Drug Design & Delivery Summit
PEPTIDE DRUG DESIGN & DELIVERY SUMMIT
December 01-03, 2020
The Peptide Drug Design & Delivery Summit will bring together key decision makers and innovators within this rapidly growing field. This intensive 3-Day program will examine various peptide discovery and synthesis techniques and synthesized and modified peptides. Hear from over 50 peptide drug c...

Annual Pharma Pricing, Reimbursement & Market Access Conference
ANNUAL PHARMA PRICING, REIMBURSEMENT & MARKET ACCESS CONFERENCE
December 02-03, 2020
Annual Pharma Pricing, Reimbursement & Market Access will bring together top pharmaceutical, biotechnology and regulatory representatives under one roof that will address the key issues of the industry. It will focus on themes such as Preparing your best market access strategy, EU and US policy ...

Annual Psychopharmacology Update
ANNUAL PSYCHOPHARMACOLOGY UPDATE
December 04-05, 2020
Annual Psychopharmacology Update features the world's leading experts who will discuss the latest advances in the pharmacotherapy of anxiety disorders, mood disorders, schizophrenia, and more.

Pharmaceutical Drug Pricing Strategies Summit
PHARMACEUTICAL DRUG PRICING STRATEGIES SUMMIT
December 09-10, 2020
The Pharmaceutical Drug Pricing Strategies Summit is designed to bring senior pricing and reimbursement leaders to discuss the future of federal and state pricing requirements, transparency regulations, and strategic drug pricing models.

American Drug Delivery & Formulation Summit
AMERICAN DRUG DELIVERY & FORMULATION SUMMIT
December 14-15, 2020
American Drug Delivery & Formulation Summit covered both small molecules and biologics, new technologies, concepts and case studies in areas such as: Formulation design for poorly soluble compounds, The potential of nanotechnology for better deliverability, The latest controlled released technol...

SPOTLIGHT

Scientists and Regulators have been sounding the alarm for missing a Disaster Plan for over three decades. We have seen several instances ranging from weather events like floods, hurricanes, earthquakes through to pandemics such as the current COVID-19 situation. Many companies found themselves not

AUG 16, 2020
DISASTER PREPAREDNESS PLAN TO SUPPORT PHARMACEUTICAL LABORATORIES DURING A PANDEMIC
Scientists and Regulators have been sounding the alarm for missing a Disaster Plan for over three decades. We have seen several instances ranging from weather events like floods, hurricanes, earthquakes through to pandemics such as the current COVID-19 situation. Many companies found themselves not ...
AUG 19, 2020 | 10.30AM
MEETING THE LATEST REGULATORY GMP REQUIREMENTS DURING CLINICAL MANUFACTURING, UNDERSTANDING KEY DIFFERENCES IN IMPLEMENTING GMPS IN CLINICAL VS. COMMERCIAL MANUFACTURING
While operating your commercial manufacturing according the GMP's can be difficult, adhering to the regulations during manufacture of materials destined for clinical trials poses even more challenges. Unlike commercial operations where operations are well defined and processes are validated, cli...
AUG 25, 2020
HOW PATIENT ASSISTANT PROGRAMS (PAPS) ARE BEING MODERNIZED WITH INNOVATIVE TECHNOLOGIES
Join us for an informative and interactive virtual panel discussion where you’ll learn about how recent trends are impacting the Patient Assistance Programs (PAP) landscape, how best-in-class PAPs incorporate multiple elements, including when/how to leverage the right technology at the right t...
SEP 01, 2020
KEY GMP REQUIREMENTS OF PHARMACEUTICAL LABORATORIES – UNDERSTANDING THE LATEST FDA & GLOBAL REGULATORY REQUIREMENTS
The Pharmaceutical laboratories serve one of the most important functions in the manufacturing of drug product. Section I of 21 CFR 211 dictates the requirements for the laboratory controls, and many laboratories consistently received 483’s and Warning Letters indicating that implementation of...
SEP 01, 2020 | 10.30AM
KEY GMP REQUIREMENTS OF PHARMACEUTICAL LABORATORIES – UNDERSTANDING THE LATEST FDA & GLOBAL REGULATORY REQUIREMENTS
The Pharmaceutical laboratories serve one of the most important functions in the manufacturing of drug product. Section I of 21 CFR 211 dictates the requirements for the laboratory controls, and many laboratories consistently received 483’s and Warning Letters indicating that implementation of...
SEP 08, 2020
ENSURING PHARMACOVIGILANCE COMPLIANCE AND ROBUST OVERSIGHT AT THE AFFILIATE LEVEL
Due to harmonisation of pharmacovigilance regulations and globalisation, the role of an affiliate has shifted to be a dual role – driving commercial growth along with pharmacovigilance management. At the same time pharmacovigilance has become more complex and operations associated with regulat...
NOV 03, 2020
OPIOID CRISIS 2020
The Opioid epidemic has been called the worst drug crisis in American history. Join us as we discuss and exchange thoughts on the rise, spread, and control of Opioids.
WEBINAR: PARTICLE ENGINEERING IN PHARMACEUTICAL SOLIDS PROCESSING
Webinar title: Particle Engineering in Pharmaceutical Solids Processing: Surface Energy Considerations Topic: This webinar presented by Dr Daryl Williams from Imperial College London reviews the surface energy and surface energy heterogeneity of crystalline solids, methods for the measurement of sur...
WEBINAR - THE 7 DEADLY SINS OF PHARMA JOB APPLICATIONS
For the last 10 years, here at GetReskilled, we have been helping people from a wide range of backgrounds make mid-career changes into well-paid jobs and careers into the pharmaceutical and medical device manufacturing industries. With a decade of experience in the industry we’ve come to learn what ...
DIGITAL BEST PRACTICES FOR ACCELERATING DRUG DEVELOPMENT
Watch this on-demand webinar to hear from Robert Albert, Collaboration Lead at AstraZeneca, and Ellen Reilly, VP of Life Sciences at DocuSign, on the digital future of pharmaceuticals and the best practices for investing and adopting eSignature solutions to reduce development cycle time and generate...
PRINCIPLES OF DIFFERENTIAL SCANNING CALORIMETRY (DSC) – THE MOST USED THERMAL ANALYSIS TECHNIQUE IN PHARMACEUTICALS
Differential scanning calorimetry (DSC) is the most frequently used thermal analysis technique alongside TGA, TMA and DMA. DSC is used to measure enthalpy changes due to changes in the physical and chemical properties of a material as a function of temperature or time. The method allows you to ident...
BIOPHARMA DEAL MAKING: LESSONS LEARNT FROM CASS BUSINESS SCHOOL’S STUDY OF STRATEGIC DEALS AND CORPORATE PORTFOLIO MANAGEMENT
Extensive prior studies have shown strong positive effects for targets and negative effects for acquirers but, they have focused on measuring value creation from individual deals, not a firm’s overall programs of activity and performance over longer time periods. This far reaching study analyzed ove...
PRACTICAL APPLICATION OF RMM IN PHARMACEUTICAL MANUFACTURING
The application of Rapid Microbiological Methods (RMM) is a topic that has gained interest over the past few years as pharmaceutical manufacturers investigate and look to gain improved efficiencies across all areas of their businesses – including the microbiology laboratory. This pharma webinar dem...
HOW TO IMPLEMENT NIR SPECTROSCOPY INTO THE PHARMACEUTICAL PROCESSES
This pharma webinar examines the technique of Near Infrared spectroscopy, and how it can be used in pharmaceutical research and development. Potential uses of this excellent PAT tool include identifying raw materials, process control testing and the examination of a final product. We also explore th...
NAVIGATING THE COMPLEXITIES OF PHARMACEUTICAL MANUFACTURING REGULATIONS
While regulatory enforcement agencies around the world have increased scrutiny on quality assurance/quality control programs, pharmaceutical manufacturers are increasingly looking for ways to lean out the manufacturing process without compromise to product quality. This push and pull conundrum has m...
THE TRUTH ABOUT PHARMACEUTICAL DRUGS AND THE MEDICAL INDUSTRY - PART 1
investigates how the influence of pharmaceutical money and guild interests has corrupted the behavior of the American Psychiatric Association and academic psychiatry during the past 35 years. He documents how the psychiatric establishment regularly misled the American public about what was known abo...
PRE-FILLED SYRINGES IN CLINICAL TRIALS
After decades of domination by small-molecule drugs, one could say that the pharmaceutical industry is increasingly thinking large. More than 60% of drugs currently in clinical development are biologics for parenteral administration.
PATIENT-CENTRIC PHARMACOVIGILANCE: BUILDING BETTER OUTCOMES THROUGH INTEGRATED TECHNOLOGY
Pharmacovigilance (PV) is the science and process of monitoring the safety of medicines, taking action to reduce the risks and increase the benefits of medicines to patients and maintaining regulatory compliance. As biopharmaceutical companies increasingly seek to achieve global patient access, ther...
SIGNAL DETECTION & TRENDING IN VETERINARY PHARMACOVIGILANCE
This webinar focuses on the process of signal detection and trending. Signal detection and trending is a powerful tool used in the management of veterinary medicines. The process of signal detection (Signal Generation, Signal Strengthening, Signal Assessment and Signal Follow-Up) can generate more s...