Assignment-3
Topic: - Cipla vs. Ranbaxy
Ranbaxy is a strong player in the Novel Drug Delivery System (NDDS) segment. Its
product portfolio spans across Acute & Chronic Business covering Anti-infective,
Nutritionals, Gastro-intestinals, Pain Management (Acute) Cardiovasculars,
Dermatologicals, Central Nervous Systems (Chronic) segments.
As we develop your strategic plan for CRM, you need to always yourself "how does this add
value to my customer and in turn add value to my company"? But you also need to keep the
following things in mind:
The process can be a lengthy one, and there are risks, especially with change management
issues. As a result, even companies who "get it" with regard to customer-centricity don't take
the steps to change their business. For those who do, success comes by going through a series
of planning stages. Here's an example:
http://www.business-standard.com/india/news/cipla%60s-
strategyhitinvestors/258363/
2) Cipla pharmaceutical creates intelligent, creative and solid visual web brands.
By seeking a coherent understanding of our clients' unique positions, business
environment, branding needs and target audience, we define a branding strategy that
captures the uniqueness of our competition.
http:// www.effective-crm-consulting.com
3) Cipla has not been able to sustain its outperformance. One of the major reasons for this
has been the muted y-o-y growth of 8.5% in domestic sales. This is lower than the
average industry growth rate of 17-18%. The drop in exports of active pharmaceutical
ingredients (APIs) also contributed to the decline in revenues. Cipla attributes this to
seasonal variations, which will get corrected over the next couple of quarters.
Its strategy shift in the export business from being a volume-driven player to a
value-conscious one has impacted its rSevenues from exports, which contribute close
to 57% to Cipla’s total revenues. Investors need to closely watch its performance
over the next couple of quarters to see how well this change plays out for the
company.
( http:// economictimes.indiatimes.com/markets/stock/stock-in-news/ciplas-portfolio-
drls.strategy-shift-to-decide-cource/articleshow/5910895)
(http://www.ibscdc.org/casestudies/strategy/core%20competency%20andcompetitive
%20advantage/CCA0004.html.)
5) Cipla's strategy has shown to be more suitable to today's scenario, in which competition
is increasing and pricing pressure is relentless. So Cipla make pricing strategy on the
base of it competitors and customer paying ability, With a ground presence in 49
countries, products available in 125 countries, and manufacturing operations in eight
countries,
3) Ranbaxy has hired 1,500 people to beef up its sales force and will launch 100 new
products in 12 months. Abbott will use Piramal’s sales force — at 7,000 — to sell existing
and new products, including patented ones.
(www.ranbaxy/casestudies.com)
4) Distribution Strategy
This strategy is used by Ranbaxy – learning about the customers purchasing products and the
behaviour of the distributers. They distribute assignments or we can say feedback form
or questionnaire and the customers and distributers get any surprise gift session, gift
after fill the forms and the company get the data about the customers.
(www.ranbaxy/casestudies/research/paper.com)
Through the various events and like Loyalty programs seminar of the health club.
LogiLabPRO:
Client : Cipla Pharmaceuticals-Pune, Enum Nostrum-Bangalore.
Language: VB
Database: Sql server
Duration: June 2009 to Till date
Testing Approach: Manual and Automation
Test Management Tool: Quality Center
Description: LogiLabPRO is instrument-interfacing software that collects data from RS232,
TCP/ IP based instrument systems. It is an RDBMS based Client/ Server, Data Acquisition,
Parsing, Archiving, Document Management, Reporting and Instrument interfacing package
for any analytical laboratory. LogiLabPRO collects data from lab instruments, a sophisticated
parsing engine extracts data of interest as fields that can be used for designing spread-sheets
and collecting data, performs calculation and seamlessly transfers data to LIMS/ ERP, has all
features to comply with GLP and 21 CFR Part 11. Archiving, Reporting, Custom Formatted
Output Software for Laboratory instruments Collect data from multiple instruments like
Balances, pH, Conductivity, Ion Meters and transferring data from logilab to LIMS.
Through the website form in which if someone want to take information then first fill his or
her information then proceed further.
Through the application form which is available with the products of Ranbaxy in which
some gifts are available if you fill the complete form and send to company address and with a
very easy question
After studying the conclusion of data acquisition of Cipla and Ranbaxy these are the
main tools. (where software is the most important tool)
TConduct BA/BE studies as per cGCP guidelines, Writing/revising SOP for clinical
operations. Review of protocols, Investigators Brochures, ICF and CRFs Protocol,
CRF and ICF preparation Plan & conduct of BA/BEIEC/IRB affairs-GC.
• Study Coordinator:
Study coordinators work directly with study volunteers, providing them safety and
protection while collecting and managing the study data. They promote, advertise, and
conduct telephone and face-to-face screenings to recruit volunteers. During the study
process, they assess volunteer condition and coordinate ongoing clinical/laboratory
testing and physical exams. Coordinators may assess vital signs (height, weight, blood
pressure, pulse), and some are trained to collect blood/urine specimens and
performing function testing. Study coordinators follow up with volunteers after the
study and manage a great deal of paperwork, electronic correspondence and data.
• Data Manager / Biostatistician:
Biostatisticians collaborate with researchers to design studies that may show the
seriousness of a disease, predict a specific disease's seriousness, evaluate a new
treatment, assess the safety and effectiveness of medications and increase knowledge
of environmental issues. Additionally, biostatisticians participate in research design,
data collection, choosing and implementing appropriate methodologies, and
interpreting the results.
Responsible for review & registration of documents as per country specific guidelines
for ex port. Evaluation of technical data & answer to various related queries as per
regulated & semi - regulated requirements. Liaison with regulatory authorities.
Conducts audits for the regulatory/QA function within the Clinical Trials Department
in order to help assure compliance with GLP/GCP in accordance with established
FDA regulations and company policies and standard operating procedures Job
Requirements Normally B.A./B.S. in Science w/1-2 years of experience.
Responsible for ensuring compliance across projects to all applicable Clinical Trial
regulations, guidelines, SOPs Protocols and procedures. Coordinate project start-up,
project maintenance and project close-out activities, Serve as the primary contact for
the Sponsor and all project team members, Direct supervisory responsibility for
project Coordinators, project Assistants, CRAs, etc
Identify potential clients & establish business relations & convert into real business.
Responsible for all Business Development functions Meeting new clients, following
up on leads, CRM. Continuously monitor the Competition and Global Market.
• Drug Safety Associate :
Manage and relay d rug safety information, maintain current knowledge of global
drug safety regulations, summaries clinical safety data, participate in meetings with
potential and actual study sponsors, write narratives with medical input from a
physician, report SADRs to the Regulatory Authorities, participate in the training of
operational staff on drug safety issues, quality control work o f other staff in the
department, take on any other task as assigned by the manager or Medical Director
within the capabilities of the Drug Safety Associate.
• Medical Writer:
The Clinical Data Manager (CDM) ensures complete, accurate and consistent data for
reporting to regulatory bodies. A CDM is involved in the setting up, running and
reporting of clinical trials. The CDM processes data using a range of computer
applications and database systems to support collection, cleaning and management of
patient data
Most businesses collect some sort of personal information on their clients, customers, or
employees. But not all of them are scrupulous in how they guard that information from theft
or misuse. Companies that keep customer or employee identification numbers, income,
personal references, employment history, health records, or other important data have a
responsibility –- in some cases, a legal responsibility –- to keep that information safe.
Privacy Policy in Ranbaxy
Ranbaxy uses its best efforts to respect the privacy of their on-line visitors. Ranbaxy only
gathers personally identifiable data, such as names, addresses, e-mail addresses, etc. when
voluntarily submitted by the user. This information is used solely by Ranbaxy, subsidiaries,
affiliates or other entities that are involved in the operation of this website for internal
purposes and is not sold or transferred to third parties. Only users who request e-mail
notification will receive same. Ranbaxy reserves the right to update this policy at any time.
(http://www.ranbaxy.com/common/privacy.aspx)
PathReports.in strives to protect th privacy of pathologists and it's customer's medical as well
personal information to the greatest possible extent. To that end, we provide the following
guidelines regarding the confidentiality of medical information:
2.) Any information concerning pathology and it's customers will be kept on highly encrypted
and secured servers. Only authorized person may ever have access to such information which
is relating to him or originated by him.
3.) Employees are hereby requested that medical information concerning employees is
absolutely confidential under state and federal laws and may not be discussed at any time
with any person under any circumstances, unless an employee needs to do so in order to carry
out his or her job duties, or unless the person discussing the information is talking or
otherwise communicating with the subject of the information at that person's invitation. If an
employee is concerned about a possible medical condition on the part of a coworker, the
employee must not discuss such concern with anyone other than [designate the person to
whom such concerns should be brought].
4.) We have provided sufficient options to the customers of pathology to maintain their
privacy which they can access in their account after signing up with a customer id or
registering with an existing customer id.You are therefore requested to change the privacy
settings if you don't wish your reports to be accessible from any where else other than only
from your account or from your registered mobile number.
CONCLUSION
After the study of Cipla and Ranbaxy I concluded that the pharmaceutical work on its
strategy according to our customer relationship management BY ED PEELEN
DIAGRAM OF CRM STRATEGY FORMULATION
Enlarge
market
Offensive
(New
Increase
Increase
customers)
Defensive Build
customer
market share
(current switching
satisfaction
customers) barriers
Generic
strategie
s
REFFERENCES
1) http://www.business-standard.com/india/news/cipla%60s-
strategyhitinvestors/258363/
2) http:// www.effective-crm-consulting.com
3) http:// economictimes.indiatimes.com/markets/stock/stock-in-news/ciplas-
portfolio-drls.strategy-shift-to-decide-cource/articleshow/5910895)
4) www.ranbaxy/casestudies/research/paper.com)
6) www.cipla.com/whatnews/newsarchive2006.html
8) WWW.GOOGLE.COM