Presentations by R. Christian Chris Moreton
           
     

Throughout his distinguished career Chris has been invited to present at various conferences, symposia, training courses and universities on excipients, dosage forms, Quality by Design and general drug development.

The presentations have been grouped by topic and venue for easier overview of the collection.

Presentations at Conferences and Symposia

Presentations about Exipients
Presentations about Dosage Forms
Presentations about Drug Development
All Presentations

Presentations at Universities and Training Courses

Presentations about Excipients
Presentations about Conventional Solid Dosage Forms of drugs
All Presentations

Presentations at Conferences and Symposia

Presentations about Excipients

Moreton R.C., Excipients to the year 2000, Formulate ‘94, Manchester, UK, (April 1994), (published in Excipients and Delivery Systems for Pharmaceutical Formulations, Karsa, D.R. and Stephenson, R.A., (Eds.), Royal Society of Chemistry Special Publication No. 161, The Royal Society of Chemistry, Cambridge, UK, (1995), 12 - 22, and also published in Pharm, Manuf. Rev., (1995), 7, (2), Pharmaceutical Formulation Supplement, S6 - S8.)

Moreton, R.C., Excipients to the year 2000, First Tablet Technology Update Symposium, Istanbul, Turkey, (April 1994).

Moreton, R.C., Tablet Excipients to the Year 2001: A Look into the Crystal Ball, 5th Annual Symposium on Solid Dosage Technology, Rutgers College of Pharmacy, Piscataway, NJ, (March 1995). (Also published in Drug Dev. Ind. Pharm., (1996), 22, (1), 11 - 23.)

Moreton, R.C., Tablet Excipients to the Year 2001: A Look into the Crystal Ball Symposium on Pharmaceutical Technology at the 1995 Conference on Pharmaceutical Science and Technology, Chicago, IL, (August 1995).

Moreton, R.C., Impurities in New and Existing Excipients - Setting Specifications and Limits, 4th International Conference on Impurities in Bulk New Chemical and Biotechnological Drug Substances and Products - Strategies and New Technologies, London, UK, (October 1995).

Çelik, M., Newman, A.W., Mueller, R., Kiesnowski, C., Vitez, I., Sharpe, S.A. and Moreton, R.C., Pre-compaction and lubrication properties of Pruv, American Association of Pharmaceutical Scientists Annual Meeting, Seattle, WA, 1996, (Pharm. Res., (1996), 13, (9 Suppl.), S-200, PT 6173).

Çelik, M., Moreton, R.C., Sherwood, B.E., Cobb, J.D., Schaible, D.J. and Zeleznik, J.A., The effects of moisture content and particle size on the functional properties of microcrystalline cellulose for use in direct compression, American Association of Pharmaceutical Scientists Annual Meeting, Seattle, WA, 1996, (Pharm. Res., (1996), 13, (9 Suppl.), S-209, PT 6212).

Moreton, R.C., Panel member for Discussion on New Excipients - From Idea to Market, 2nd Symposium on Macromolecules used as Pharmaceutical Excipients - New Opportunities, Characterization and Applications, Stockholm, Sweden, (February 1997),

Moreton, R.C., Prospects for new excipients for oral solid dosage forms, IIR Conference: Latest Developments in Solid Dosage Form Technology, Orlando, FL (December 1997).

Moreton, R.C., Challenges in the selection of new excipients for oral solid dosage forms, Symposium on Pharmaceutical Technology at the 1998 Conference on Pharmaceutical Science and Technology, Dallas, TX, (April 1998).

Moreton, R.C., Prospects for new excipients for oral solid dosage forms IPEC-Europe Conference, Nice, France (May 1998).

Moreton, R.C., Prospects for new excipients for oral solid dosage forms, IIR Conference: Recent Developments & cGMP Advances for Pharmaceutical Solid Dosage Forms, Princeton, NJ (May 1998).

Moreton, R.C., What’s new in excipients: Prospects for new excipients for oral solid dosage forms, WORLDPHARM98 Conference: Philadelphia, PA (September 1998).

Moreton, R.C., Excipients, a General Overview, ICH Impurity Guidelines: In Theory and in Practice: Lake Buena Vista, FL, (April 1999).

Moreton, R.C., IPEC Audit Guidelines for Manufacturing and Distribution, Pharmaceutical Excipients Conference: Philadelphia, PA (April 2000).

Steele, F., Edge, S., Moreton, C., Tobyn, M.J. and Staniforth, J.N., Effect of source of microcrystalline cellulose on adsorption of amine drugs, American Association of Pharmaceutical Scientists Annual Meeting, Indianapolis, IN, 2000, Presentation no. 1285.

Steele, F., Edge, S., Moreton, C., Tobyn, M.J. and Staniforth, J.N., Factors affecting the adsorption of amine drugs by microcrystalline cellulose, 20th Pharmaceutical Technology Conference and Exhibition, Liverpool, UK (April 2001).

Moreton, R.C., Characterization of excipients and their interaction with active drugs, IIR Conference: Pharmaceutical Excipients: Strategies for Meeting Regulatory and Technical Challenges, Philadelphia, PA, (August 2001)

Steele, D.F., Edge, S., Wolverson, D., Moreton, R.C., Tobyn, M.J. and Staniforth, J.N., The use of UV-Raman microscopy and infrared spectroscopy to investigate inter-brand variations in microcrystalline cellulose, American Association of Pharmaceutical Scientists Annual Meeting, Denver, CO, 2001, Presentation no: M2168.

Steele, D.F., Edge, S., Reutenauer, S., Thielmann, F., Moreton, R.C., Tobyn, M.J. and Staniforth, J.N., Comparison of inverse gas chromatography and capillary intrusion in the determination of the surface energy of microcrystalline cellulose samples, American Association of Pharmaceutical Scientists Annual Meeting, Denver, CO, 2001, Presentation no: W4551.

Moreton, R.C., The Purpose and Layout of Pharmacopeial Monographs for Excipients, USP - IPEC-Americas Joint Conference on Pharmaceutical Excipients, Fort Myers, FL, (December 2001).

Moreton, R.C., The Purpose and Layout of Pharmacopeial Monographs for Excipients, IPEC-Americas Regulatory Affairs Conference, Bethesda, MD, (September 2002).

Moreton, R.C., Some Considerations Relating to the Development of New Excipients, EUFEPS Annual Congress 2002, Stockholm, Sweden, (October 2002)

Moreton, R.C., An Update on Excipient Harmonization Activities, AAPS Annual Meeting 2002, Toronto, ON, Canada, (November 2002).

Brittain, H.G., Schoneker, D.R. and Moreton, R.C., Reference Standards for Excipient Monographs, USP/FebraFarma/Farmacopeia Brasileira Conference on Pharmaceutical Excipients, Sao Paulo, Brazil, (November 2002).

Moreton, R.C., Future of Excipient Technology: The Vendor’s Perspective, University of Wisconsin – 46th Annual International Industrial Pharmaceutical Research and Development Conference: Pharmaceutical Excipients: Role of Excipients in Solubility and Bioavailability Enhancement: Current Approaches, Unmet Needs and Future Challenges, Merrimac, WI, (June 2004).

Moreton, R.C., Impurities in Excipients, Quality on the move: Dynamics of the European Pharmacopoeia, International Conference, Budapest, Hungary, (4 - 6 October, 2004).

Moreton, R.C., Functionality-related Characteristics, IPEC-Americas 15th Anniversary Conference, Orlando FL, (January 26 - 27, 2006)

Moreton, R.C., Excipients, Functionality and Functionality-related Characteristics: An Excipient Manufacturer’s Perspective, NIPTE Workshop, Gaithersburg, MD (April 5 - 7, 2006)

Moreton, R.C., Functionality and Performance of Excipients, Pharm Tech Annual Event, Somerset, NJ, (June 12 - 15, 2006).

Moreton, R.C., Performance Tests for Excipients: An Industrial Perspective, United States Pharmacopeia Annual Scientific Meeting, Denver CO (September 26 - 29, 2006).

Moreton, R.C., Additives and Impurities in Excipients: An Expert Committee Perspective, United States Pharmacopeia Annual Scientific Meeting, Denver CO (September 26 - 29, 2006).

Moreton, R.C., Functionality and Performance of Excipients, SWE Pharmaceutical Excipients Conference, La Jolla, CA (January 2007).

Moreton, R.C., Additives and Impurities in Excipients, SWE Pharmaceutical Excipients Conference, La Jolla, CA (January 2007).

Moreton, R.C., Working with Contract Manufacturers, Pharmaceutical Technology Annual Conference, Philiadelphia, PA (July 2007)

Moreton, R.C., Excipient Composition: Relevance and Impact United States’ Pharmacopeia Annual Scientific Meeting, Tampa, FL (September 2007).

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Presentations about Dosage Forms

Tan, S.B., Moreton, R.C. and Smith, D., Flow properties and tablet weight uniformity: Effects of granule size and machine speed, British Pharmaceutical Conference 1979, Exeter, UK, (J. Pharm. Pharmacol., (1979), 31, (Suppl.), 74P.)

Moreton, R.C., Application of Theory to the Optimization of Enteric Coating, Symposium on the Theory and Practice of Film Coating, Solid Dosage Research Unit, Liverpool, UK, 1980.

Armstrong, N.A., Gebre Mariam, T., Moreton R.C. and Thompson, H.J., The influence of gelatin hydrolysis on diffusion through glycerogelatin gels, British Pharmaceutical Conference 1990, Cardiff UK, (J. Pharm. Pharmacol., (1990), 42, (Suppl.), 4P.)

Armstrong, N.A., James, K.C., Moreton, R.C. and Morton, F.S.S., Diffusion of volatile hydrophilic substances through glycerogelatin films, British Pharmaceutical Conference 1990 Cardiff, UK, (J. Pharm. Pharmacol, (1990), 42, (Suppl.), 5P.)

Moreton, R.C. and Armstrong, N.A., An apparatus for measuring diffusion through glycerogelatin films, American Association of Pharmaceutical Scientists Annual Meeting, San Diego, CA, 1994, (Pharm. Res., (1994), 11, (10 Suppl.), S-147, PT 6066).

Liu, L., Sackett, G.L., Smith, T.J., Goldsberry, T.J., Moreton, C. and Baichwal, A., The effect of load volume on a novel controlled release system in a high shear granulator, American Association of Pharmaceutical Scientists Annual Meeting, Indianapolis, IN, 2000, Presentation no. 1079.

Moreton R.C., Pharmaceutical Development and Manufacturing: Trends in Processing of Oral Solid Dosage Forms, PharmSciFair, Nice, France (June 2009).

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Presentations about drug development (general)

Moreton, R.C., Working with less API: A Perspective from Management, IIR Formulation Development Conference, Philadelphia, PA, (July 26 - 27, 2005).

Moreton, R.C., Product Development in a Virtual Company, AAPS Annual Meeting, San Antonio, TX (October 2006).

Moreton R.C., Pharmaceutical Materials: What Can We Do To Confirm Their Integrity?, AAPS Annual Meeting, Atlanta, GA (November 2008)

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Presentations at Universities and Training Courses

Presentations about Excipents

University of Connecticut - Storrs, CT, visiting lecture ‘Excipients, Functionality and Functionality-related Characteristics’, February 2006.

Moreton, R.C., Compendial Requirements for Excipients and International Harmonization, Pre-conference Workshop IIR - 2nd Annual Conference on Drug-Excipient Compatibility Studies, Princeton NJ (March 20 - 21, 2006).

Moreton R.C., Excipient Supply Chain Issues: an Overview. USP International Excipient Workshop, Rockville, MD (July 2009).

Moreton R.C., Excipients in Quality by Design: Myths and Realities. USP International Excipient Workshop, Rockville, MD (July 2009).

Moreton R.C., The Influence of Excipient Functionality on Quality by Design for Drug Products: The Excipient Manufacturer’s Perspective. AAPS Annual Meeting, Los Angeles, CA (November 2009).

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Conventional Solid Dosage Forms of drugs.

University of Wisconsin - Madison, Pharmaceutical Engineering and Technology Series, Advanced Practices in Pharmaceutical Tablet and Capsule Technology, May, 2003, 2004 and 2005, Las Vegas, NV; Use of the Major Tablet and Capsule Excipients: Properties, Advantages and Disadvantages and the Trends in Their Usage.

European Continuing Education College, UK, Short course: Principles of Tablet and Capsule Formulation, 2005, Excipients and Preformulation.

European Continuing Education College, UK, Course: Design and Development of Conventional and Modified Release Oral Drug Delivery Systems, April 2007; Preformulation.

De Montford University, Leicester, UK, visiting lecturer on Excipients for Solid Dosage Forms, 1992/3 and 1993/4.

University of Lille, France, visiting lecturer on Excipients for Direct Compression, 1992/3, 1993/4 and 1994/5.

The Welsh School of Pharmacy, University of Wales College of Cardiff, UK, visiting lecturer on Excipients for Direct Compression, 1993/4 and 1994/5.

University of Cincinnati, OH, visiting lecturer on Excipients for Solid Dosage Forms, 1994, 1995 and 2001.

University of Cincinnati, OH, visiting lecturer on Excipients for Oral Controlled Release Solid Dosage Forms, 1999 and 2001.

University of Wisconsin - Madison, Pharmaceutical Engineering and Technology Series, Fundamentals and Advanced Practices in Pharmaceutical Tableting, May 17 - 19, 1999 Las Vegas, NV; Ingredients used in the Development of Solid Dosage Forms: Part 1 - Ingredient Compatibility, and: Part 2 - Important Physical Properties and Parameters.

The University of Greenwich, UK, visiting lecturer on Preformulation Studies, 1994

University of Wisconsin - Madison, Pharmaceutical Engineering and Technology Series, Fundamentals and Advanced Practices in Pharmaceutical Tableting, May 20 - 22, 2002 Las Vegas, NV; Excipients in Oral Immediate Release Solid Dosage Forms.

University of Wisconsin - Madison, Pharmaceutical Engineering and Technology Series, Advanced Practices in Pharmaceutical Tablet and Capsule Technology, Las Vegas, NV; Pharmaceutical Excipients: Uses and Recent Developments, May 2006 and May 2007.

European Continuing Education College, UK, Course: The Formulation of Tablets and Capsules, 2008, Quality by Design and Formulation Design and Development.

University of Kuopio, Finland, Visiting lecture –Trends in Pharmaceutical Product Development and Manufacture, October 2008.

University of Kuopio, Finland, Visiting lecture –Future needs in pharmaceutical development and manufacturing, September 2009.

Center for Professional Advancement, in-house 3-day training course (sole presenter): Formulation and Development of Chiral Drugs, Sarajevo, Bosnia, February 2009.

Center for Professional Advancement, Course: Granulation, Tableting and Capsule Technology, Amsterdam, NL; Design and Development of Tablet Formulations, May 2009.

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