In 2005, Phillip (Phil) Landgraf faced several glaring problems in the financial performance of his company, BioPharma, Inc. The firm had experienced a steep decline in profits and very high costs at its plants in Germany and Japan. Landgraf, the company 's president for worldwide operations, knew that demand for the company 's products was stable across the globe. As a result, the surplus capacity in his global production network looked like a luxury he could no longer afford.
Any improvement in financial performance was dependent on having the most efficient network in place, because revenues were unlikely to grow.. Cutting costs was thus a top priority for the coming year. To help design a more cost-effective network, Landgraf assigned
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Local production within each region is assumed to result in no import duty. Thus, production from Brazil, Germany, and India can be sent to Latin America, Europe, and the rest of Asia without Japan, respectively, without incurring any import duties. Duties apply only to the raw material, production, and transportation cost component and not to the fixed cost component. Thus, a product entering Latin America with a raw material, production, and transportation cost of $10 incurs import duties of $3.
NETWORK OPTIONS UNDER CONSIDERATION
The task force is considering a variety of options for its analysis. One option is to keep the global network with its current structure and capabilities. Other options include shutting down some plants or limiting the capability of some plants to producing only one chemical. Closing down a plant eliminates all variable costs and saves 80 percent of the annual fixed costs (the remaining 20 percent accounts for costs that are incurred related to the plant shutdown). Similarly, if a plant is limited to producing only one chemical, the plant saves 80 percent of the fixed cost associated with that particular chemical. The two options being seriously considered are shutting the Japanese plant and limiting the German plant to a single chemical.
QUESTIONS
1. How should BioPharma have used its production network in 2005? Should any of the plants have been
The required safety stock levels can be found in columns BD, BE, and BF. BH, BI, and BJ columns provide the DC product inventory averages necessary to have a 95 percent service level. Based on the standard cost, column BK converts the average inventory units into average dollars. As you can see, it will require the company to have $7.5M to achieve a 95 percent fill rate while the current situation has a 96+ percent service with double the inventory.
Pharma Co. should account for the restructuring program in different ways for the U.K parent and to U.S.-based lender.
Production operations played a huge role on whether to allow more production in North America, or more in Europe-Africa. After many decisions, we begun to notice that North America, and Europe-Africa were our main consumers and had stronger demands for our products, we suddenly realized that we should offer the other more compensation to raise the production. We than decided to offer Asia-Pacific, and Latin America a larger discounts, and longer return dates, to increase the demands.
The management team at the over-the-counter cold medicine (OCM) group of Allstar Brands is looking to utilize revenue generated by Allround to help fund new opportunities in emerging markets. Therefore, it is critical that Allround maintain its market-leading position in terms of market share, profitability, and sales in order to fund these new initiatives.
The Pharmaceutical industry has been in the spotlight for decades due to the fact that they have a reputation for being unethical in its marketing strategies. In The Washington Post Shannon Brownlee (2008) states, “We try never to forget that medicine is for the people. It is not for the profits. The profits follow.” This honorable statement is completely lost in today’s world of pharmaceutical marketing tactics. These tactics are often deceptive and biased. Big Pharma consistently forgets their moral purpose and focuses primarily on the almighty dollar. Big Pharma is working on restoring their reputation by reforming their ethical code of conduct.
The need of the application for an NDA or ANDA and CGMPs to compounded PET drug products in which FDAMA is concerned are implemented by two reports such as the Joint Explanatory Statement of the Committee of Conference issued by the House of Representatives on November 9, 1997, and a Senate report published on July 1, 1997. The Senate report consists of a more detailed information regarding the clinical importance of PET molecular imaging and an ideal option of a regulatory framework for PET radiopharmaceuticals. The report indicates that Section 619 (the Senate's version of Section 121 of FDAMA) is intended to provide a new framework for the regulation of PET drugs based on the standards set by
On December 13, 2012, Vertical Pharmaceuticals Inc., a privately owned company that sells niche prescription drugs geared toward women’s health and pain management, and an affiliated company sued Deloitte & Touche LLP in New Jersey state court for alleged accountant malpractice. Deloitte’s false accusation led to the withdrawal of another public company's planned acquisition of Vertical. If the deal completed, Vertical would be extremely beneficial from the acquisition because the public company would help its business and would achieve generous profits of $500 million or more. According to the complaint, Deloitte discontinued the audit of Vertical and Trigen Laboratories financial statement for 2011 and then resigned from the
Medtech Pharmaceuticals is a new drug company that just got approved by the FDA for developing a drug used to treat melanoma (Johnston & Marshall, 2010). The goal of the company is to spread out the new drug to various regions around the country. The success of MedTech is the fact the drug can treat melanoma, a form skin cancer, without surgery. The growing amount of baby boomers in America will eventually come under the condition of some form of skin cancer during their lifetime.
MedTech Pharmaceuticals began with great potential and knowledgeable individuals who could make this company a success. Doug Reynolds, founder of MedTech Pharmaceuticals had a vision; therefore, changing his position from research and venturing in a new direction seemed to be the right move (Johnston & Marshall, 2009). Additionally, Doug had the expertise in the drug makeup from his molecular biology background; thus, Doug chose to make two drug compounds to treat skin cancers (Johnston & Marshall, 2009).
How well do you know your pharmaceutical provider? This research paper will closely examine Valeant Pharmaceuticals International Inc issues and market regarding The New York Hotel Trades Council & Hotel Association of New York City Inc Health Benefits Fund et al v. Valeant Pharmaceuticals International Inc et al, U.S. District Court, Southern District of New York, No. 16-06779 case.
After review of the primary issue it has been discovered that (in accordance with both U.S. GAAP and IFRSs guidelines) Pharma Company’s plan to relocate its manufacturing operation meets the criteria
The case study titled “Will Mannkind’s Dream Come True?” highlights many existing problem(s) faced by the company. It also provides a framework to analyze scenarios, which could help us to determine what could be the best strategy for them to adopt in order to become a profitable and successful Biotech (Drug development) company. By comprehensive PESTEL (PESTLE) Analysis, the case study provided various external factors that affect any biotech company in general. These factors are particularly important for analyzing MannKind’s positions as they posse direct impact on the organization and the key decision maker for the company, and may also affect at arriving at the recommendation for the key problem.
* 1. Case Study Kramer Pharmaceuticals, Inc. Presented by Debi Prasad Bagria Kishor Chandwani Nandini Mudgil Mrinmoy Kanti Das Rahul Agarwal Ritesh Kumar Singh
1. How has Merck been able to achieve substantial returns to capital given the large costs and lengthy time to develop a new drug?
Following the supply chain review GSKs decided to change the planning management system and replenishment system. The purpose was to substitute the traditional CMI with Vendor Managed Inventory (VMI).