Insight Briefing Schedule

What is an Insight Briefing?

Insight Briefings are in-depth seminars on technical and business topics right on the CPhI North America exhibition floor, accessible to all exhibition visitors. Topics include accelerated drug approval programs, the digital transformation of the pharmaceutical industry, supply chain security advancements and much more!

Schedule At A Glance

 

 Tuesday, May 16Wednesday, May 17Thursday, May 18
Time   
10:30 AMOrbis BiosciencesGSK/GlaxoSmithKlineSafeBridge Consultants, Inc.
11:30 AMGE Life SciencesDitebaNSF International
12:30 PMShenyang Gold Jyouki Technology Co., LtdPiramal (Ash Stevens) Haig Barrett
1:30 PMSikichAnsell American Chemical Society
2:30 PMUnither PharmaceuticalsPharmaceutical Technology and BioPharm International 
3:30 PMAvista Pharma Solutions, Inc. DPS Consulting  
4:30 PM Catalent 

Cory Berkland, PhD, Chief Scientific Officer, Orbis Biosciences 

Leveraging Controlled Release Powders to Create Patient-Friendly Products.

Tuesday, 10:30 AM - 11:15 PM

Orbis Biosciences

The rising cost of healthcare and the resultant shift of policies focused on lowering costs and incentivizing better outcomes are driving increased demand for drug delivery solutions that can improve patient compliance and provide economical solutions for special patient populations such as pediatrics and geriatrics. Controlled release solutions play a critical role in patient-centric design, offering the ability to reduce the number of administrations required by the patient. In this session we will explore fabrication techniques for controlled release powders and the role they can play in creating patient-friendly products.

Andrea Hamilton, Senior Scientist, Fast Trak Services

Faster to Market—Case Study on Successful Process Development, and Technical Transfer

Tuesday, 11:30 AM - 12:15 PM

GE Life Sciences

Whether you’re looking to launch a new molecule, enhance existing capacity or bring biosimilars to emerging markets, developing process development skills in key enabling technologies are critical to the long term success of your product. This presentation will focus on a key case study focusing on development and optimization of a biopharmaceutical product, while at the same time ensuring it is of the same quality and is manufactured in a reproducible manner.  We will demonstrate how ensuring you identify critical process parameters early on and maintaining those parameters through scale up can ensure you avoid needless process steps later on and increase the overall efficiencies for manufacturing.

Xiao-Bing Lu, Shenyang Gold Jyouki Technology Co., Ltd

CO2-Mediated Formation of Chiral Fine Chemicals

Tuesday, 12:30 - 1:15 PM

Shenyang Gold Jyouki Technology Co., Ltd

The utilization of carbon dioxide as a feedstock for the synthesis of organic chemicals can contribute to a more sustainable chemical industry, since CO2 is an abundant, inexpensive and non-toxic renewable C1 resource. Nevertheless, far less attention was paid to the stereochemically controlled catalytic CO2 fixation/conversion processes. The presentation therefore aims to principally showcase of the recent progress regarding CO2 mediated formation of chiral fine chemicals, including enantioselective synthesis of cyclic carbonates by asymmetric ring-opening of epoxides with CO2, enantioselective synthesis of oxazolidinones by the coupling reaction of aziridines with CO2 and enantioselective synthesis of CO2-based polycarbonates from epoxides, as well as chiral diols and carbamates via polycarbonate intermediates.

Debbie Altham, Industry Director, SIKICH

Digital Transformation in the Chemical and Life Sciences Industries

Tuesday, 1:30 - 2:15 PM

Sikich

Technology is playing an increasing role in everything we do. In the chemical and allied industries, digital technologies provide actionable solutions to business challenges, and groundbreaking opportunities for innovation. Come and hear Debbie Altham, Industry Director from professional services and technology firm SIKICH, explore overall business trends in the industry and how digital transformation presents new opportunities for business leaders to harness the disruptive force of technology to be more agile, drive efficiency, and ultimately help shape their destiny.

Dr. Hanumantharao Tatapudy, Executive Director of Research and Development, Unither Pharmaceuticals

Unit Dose Solving an Unmet Need in the Pharma Industry via Liquid Stick packs and Blow-fill-seal – the wings of a CDMO

Tuesday, 2:30 - 3:15 PM

Unither Pharmaceuticals

“Unit dose” is the name of the game in today’s Pharma World and this will be a game changer – The Wings of a CDMO. Measuring caps, tablespoons, teaspoons and multiple dose containers for Oral Liquids and Eye drops are a thing of the past. Today’s patient is looking for convenience and Doctors are also realizing the value of unit dose with regard to writing prescriptions. Parents and caretakers of children and Geriatrics whether at home or in a hospital /nursing home are seeing the benefit of not having to measure an oral liquid plus not having to share an oral liquid bottle or have a Doctor write multiple prescriptions of the same medicine to cover home and school, etc. It also allows doctors to now be able to write prescriptions for controlled substance oral liquids as unit doses addressing the abuse issue. It also allows Pharmacists to store the oral liquids under lock and key – a great new advantage that does not exist today. Best of all it opens the doors to almost any unit dose oral solid or multiple dose oral liquid to be converted to a unit dose oral liquid to address several challenges including stability concerns related to multiple dose oral liquids such as light sensitivity and oxygen head space. The benefit of introducing ophthalmics as unit dose without preservatives is an immense advantage in addition to the convenience of transportation. Today’s world of nebules to be used for Inhalation is governed by unit dose and is a great patient convenience. Just imagine the convenience of being able to have a few Liquid stick packs of your favorite Cough-Cold-Fever medicine readily available in your Laptop bag or purse and not needing to worry about leaving the whole bottle behind after a trip or while going on a trip. Also, the convenience of being able to share the same medicine with other family members and literally take it in any setting without having to worry about measuring it. This enhances patient medication compliance and adherence to medication schedule and eliminates medication dosing errors due to several reasons including the most ignored one- language barriers to read and understand instructions on labels especially for OTC products wherein a Pharmacist may not be engaged in explaining the dosing directions.

Tuesday, 3:30 - 4:15 PM

Avista

Scott Goodberlet, Quality Director, North America Supply Chain, GSK

Managing Implications Stemming from Regulatory Observations

Wednesday, 10:30 - 11:15 PM

GSK

Dr. Theo Kapanadze, Ph.D. Chief Scientific Officer, Diteba

In Vitro Approach to Qualify Acyclovir Cream Products for Biowaiver Status

Wednesday 11:30 - 12:15 PM

Diteba

In accordance with the recently released FDA draft guidance on acyclovir, Diteba presents on a fully compliant approach that combines the extensive acyclovir in vitro release testing (IVRT) and in vitro skin permeation testing (IVPT). This approach provides drug companies with the optimal chance of biowaiver success in lieu of the high cost and long delivery times associated with human clinical trials.

Sean P. Lapekas, Senior Process Safety Engineer, Ash Stevens, LLC

Effective Process Safety Evaluations for CDMO API Operations

Wednesday, 12:30 - 1:15 PM

Piramal

Besides addressing the technical challenges associated with executing synthetic organic chemistry on progressively larger scales, the process safety risks must also be fully assessed and understood. API manufacturing processes often utilize exothermic reactions in flammable solvents. In addition, the API and/or intermediate structures may contain functional groups associated with high energy decomposition. Failure to adequately address these hazards can have a devastating impact on a CDMO, their employees, their clients, and the surrounding community. This presentation will review the work-flow and test instruments available for performing thorough process safety assessments.

George Turner, Senior National Accounts Manager, Ansell

Laboratory and Production Environments in Life Science

Wednesday, 1:30 - 2:15 PM

Ansell

The life science industry faces the toughest challenges from a quality and regulatory perspective. In typical laboratory environments the researcher faces chemical, biological and mechanical hazards. The suitable selection of a barrier that provides appropriate hazard protection is crucial. In a production environment this barrier performs a dual function of protecting the researcher as well as protecting the product. In this presentation we will discuss Ansell’s innovative offering designed to meet your stringent requirements across all environments. Ansell’s proprietary solutions tool “Chemical Guardian” is a great asset which recommends optimal glove selection

Rita Peters & Agnes Shanley | Editorial Director & Senior Editor 

Quality Practices: Meeting and Exceeding Regulatory Expectation

Wednesday, 2:30 - 3:15 PM

Pharmaceutical Technology and BioPharm International

Aging equipment, supplier errors, inadequate QA/QC practices, and other factors can contribute to quality problems and regulatory action for drug companies and contract service providers. The editors of Pharmaceutical Technology and BioPharm International, in conjunction with CPhI North America, conducted an industry-wide survey of the state of quality practices at companies manufacturing drugs for the US market.

The survey results, which will be released during this session, reveal current quality-related practices in bio/pharma organizations and contract manufacturers producing drug products for patients in the US. Respondents share insight on interactions with regulatory authorities, quality challenges, and supplier oversight. The responses identify areas of best practices and areas needing improvement for bio/pharma companies, contract service providers, and regulatory authorities

Ahmed Elsawah, President, DSP Consulting 

Pharma Opportunities and Innovative Business Models in MENA Region

Wednesday, 3:30 - 4:15 PM

DSP Consulting

Middle East North Africa region has never been the same for all countries in the region.Business potential of pharma industry and regulations  are very much varying.As a result,only four countries are representing 80% of business potential and double digit growth rates. The objective of that briefing is to shed enough light on that lucrative growing market and pinpoint target therapy areas and best successful precedented business models.

Wednesday, 4:30 - 5:15 PM

Catalent

Charlyn Reihman & Allan Ader | Principal Occupational Health Consultant & Managing Director

What Does it Take to Manufacture Potent Compounds?

Thursday, 10:30 AM - 11:15 AM 

Safebridge Consultants, Inc.

As more highly potent active pharmaceuticals make the way to the research laboratories and eventually the marketplace, a multi-faceted approach is necessary to reduce occupational risk around handling these active pharmaceutical ingredients (API). As patients benefit from the reduced risk of adverse effects and target specific drugs, employees in all phases of manufacturing are at increased risk. SafeBridge will present a comprehensive approach for hazard identification and risk reduction during various phases of API and pharmaceutical manufacturing. Included will be a discussion of the “alphabet soup” of risk assessment terminology needed to successfully work with these compounds including OEB, OHC, OEL, ADE, PDE, and ASL, and the importance of quantitative data in assessing occupational exposure risk.

Thursday, 11:30 AM - 12:15 AM

NSF International

Haig Armaghanian, Founder, CEO and Chief Visionary Officer

Hitchhikers Guide to Leveraging M&A in the Pharma Galaxy

Thursday, 12:30 PM

Haig Barrett

Over the past few years, M&A has fueled hyper-accelerated growth within the Global Pharma industry, here at CPhI North America, Haig and his insightful team will share their experience and collective wisdom about the current climate. In addition to helping you identify ways to navigate through the major challenges of the post-merger integration terrain, you will also get a peak at the future state of the industry with the balance of influence ever-shifting between Big Pharma, CMO/CDMO/CRO and the growing cadre of small innovators.

Jane Arrington, Product Manager, CAS, a division of American Chemical Society 

Best Practices for Reducing Regulatory Risk

Thursday 1:30 PM 

American Chemical Society

Researching regulatory status can be difficult and time-consuming, and the safety and financial risks of missing key information can be critical to the success of your business.  Searches must be accurate and thorough to include all the ways substances are identified scientifically and commercially around the world.  From a unique CAS Registry Number to a trade name, your business depends on the ability to navigate the regulatory environment for the chemicals you produce, use, transport or sell.

Join us as we describe and demonstrate search techniques that help ensure regulatory searches are both precise and comprehensive.  We’ll also cover how CAS Registry Numbers and substance names are assigned, why some registrations may not include CAS RNs, and resources you can tap to quickly get the information you need when registering substances with regulatory authorities.