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Posts from ‘January, 2009’

Johnson and Johnson Completes Delicate Offer for Mentor Corporation

NEW BRUNSWICK, N.J., Jan. 23 (HSMN NewsFeed) — Johnson & Johnson (NYSE: JNJ ) today announced the expiration of the subsequent offering period of the cash tender offer through its wholly owned subsidiary, Maple Merger Sub, Inc., for all excellent shar…
Devices, Mergers & Acquisitions
Johnson & Johnson, Mentor Corp

Geron Receives FDA Clearance to Begin World’s First Human Clinical Trial of Embryonic Stem Cell-Based Therapy

Geron to Study GRNOPC1 in Patients with Acute Spinal Cord Injury MENLO PARK, Calif., January 23, 2009 - (HSMN NewsFeed) - Geron Corporation (Nasdaq: GERN) announced today that the U.S. Food and Drug Administration (FDA) has granted clearance of the comp…
Regenerative Medicine, Neurosrugery, FDA
Geron Corp, GRNOPC1, spinal cord injury, human embryonic stem cell

Mylan Receives Final FDA Approval for Generic Version of Prilosec(R) Delayed-Release Capsules, 40 mg

PITTSBURGH, Jan. 23 (HSMN NewsFeed) — Mylan Inc. (Nasdaq: MYL ) today announced that its subsidiary Mylan Pharmaceuticals Inc. received final approval from the U.S. Food and Drug Administration (FDA) for its supplemental Abbreviated New Drug Application…
Biopharmaceuticals, Generics, FDA
Mylan, Omeprazole, AstraZeneca, Prilosec, gastroesophageal reflux disease

IMPAX Receives Final FDA Approval for Omeprazole Forty mg Capsules

Marketing to Begin Immediately HAYWARD, Calif.–(HSMN NewsFeed)– IMPAX Laboratories, Inc. (OTC: IPXL), through its generic drug division Global Pharmaceuticals, announced that yesterday the U.S. Food and Drug Administration (FDA) granted final approval…
Biopharmaceuticals, Generics, FDA
IMPAX Laboratories, Omeprazole, AstraZeneca, Prilosec, gastroesophageal reflux

Merck Serono’s Oral Investigational Treatment Cladribine Tablets for Multiple Sclerosis Significantly Reduced Relapse Rate in Two-Year Phase III Pivotal Trial

- Two-Year Primary Efficacy Endpoint of CLARITY Trial met: 58% Relative Reduction in Annualized Relapse Rate in the low Total Dose Treatment Group and 55% in the High Total Dose Treatment Group - Submission for Registration of Cladribine Tablets Planned fo…
Biopharmaceuticals, Neurology
Merck Serono, Merck KGaA, cladribine, multiple sclerosis, CLARITY study

Geron Receives FDA Clearance to Begin World’s First Human Clinical Trial of Embryonic Stem Cell-Based Therapy

Geron to Study GRNOPC1 in Patients with Acute Spinal Cord Injury MENLO PARK, Calif., January 23, 2009 - (HSMN NewsFeed) - Geron Corporation (Nasdaq: GERN) announced today that the U.S. Food and Drug Administration (FDA) has granted clearance of the comp…
Regenerative Medicine, Neurosrugery, FDA
Geron Corp, GRNOPC1, spinal cord injury, human embryonic stem cell

Lytix Closes USD Ten.4 Million Funding Round

Antimicrobial and Oncology Lead Compounds to be Taken Through Early Clinical Development TROMS0, Norway, January 22 (HSMN NewsFeed) — The Scandinavian-based drug development company Lytix Biopharma today announced the closure of a successful funding …
Biopharmaceuticals, Venture Capital
Lytix Biopharma, antibiotic

Isotechnika Announces Full Enrollment Achieved in Partner Atrium’s CONFIRM 1 Trial for Voclosporin Coated Coronary Stent System

EDMONTON, Jan. 22 - (HSMN NewsFeed) - (ISA:TSX): Isotechnika Inc. announced today that its partner, Atrium Medical Corporation has completed patient enrollment for their CONFIRM 1, First-in-Man (FIM) drug coated coronary stent clinical trial evaluating Atr…
Devices, Interventional Cardiology
Isotechnika, Atrium Medical, CONFIRM 1, CINATRA, voclosporin, stent, FIM trial

Cardo Medical Announces the Initial Release of Its Press-Fit Total Hip System

LOS ANGELES, CA–Jan 22, 2009 — Cardo Clinical (OTC BB:CDOM.OB ), a company engaged in the development of orthopedic medical devices, announces the initial release of its Press-Fit Total Hip system. The Press-Fit Total Hip system incorporates a dual taper …
Devices, Orthopaedic
Cardo Medical, Press-Fit, Total Hip, hip replacement

New Biologic STELARA(TM) Receives Approval in Europe for Treatment of Moderate to Severe Plaque Psoriasis

First and Only Biologic Approved with Infrequent, Every Twelve-Week Maintenance Dosing BEERSE, Belgium, Jan. 22 (HSMN NewsFeed) — Janssen-Cilag announced today that STELARA(TM) (ustekinumab), the first in a new class of biologics, has been approved b…
Biopharmaceuticals, Regulatory
Janssen-Cilag, STELARA, ustekinumab, severe plaque psoriasis, psoriasis